Datasets:

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Q40.93
Q40
Are there any specific alleles within the gene ALDH9A1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain and Putamen Basal Ganglia samples tested, there are no alleles within the gene ALDH9A1 that are significantly associated with an increased susceptibility to ...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ALDH9A1' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1937
Q40
Are there any specific alleles within the gene PRKCB associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene PRKCB that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'PRKCB' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1215
Q40
Are there any specific alleles within the gene CTD-2377O17.1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene CTD-2377O17.1 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CTD-2377O17.1' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.882
Q40
Are there any specific alleles within the gene RP11-503C24.1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene RP11-503C24.1 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-503C24.1' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1353
Q40
Are there any specific alleles within the gene CRNN associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Blood and Cortex samples tested, there are no alleles within the gene CRNN that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CRNN' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1891
Q40
Are there any specific alleles within the gene STARP1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene STARP1 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'STARP1' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1102
Q40
Are there any specific alleles within the gene HNRNPA1P70 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene HNRNPA1P70 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'HNRNPA1P70' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1165
Q40
Are there any specific alleles within the gene MIR200C associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene MIR200C that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'MIR200C' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1365
Q40
Are there any specific alleles within the gene PPP1CA associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene PPP1CA that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'PPP1CA' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1959
Q40
Are there any specific alleles within the gene C12orf5 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Cerebellar Hemisphere, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Liver, Whole Blood, Cerebellum and Nucleus Accumbens Basal samples tested, there are no alleles within the gene C12orf5 that are significantly associated with an increased susceptibilit...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'C12orf5' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.505
Q40
Are there any specific alleles within the gene WDR18 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene WDR18 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs2240149 • Multi Ancestry Whole Brain: Adjusted SMR multi-SNP P-value: 4.87e-07; b: 2.1243e-02
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'WDR18' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1397178', 'Gene': 'WDR18', 'Omic_tissue': 'Multi Ancestry Whole Brain', 'topSNP': 'rs2240149', 'A1': 'A', 'A2': 'G', 'Freq': 0.599182, 'p_SMR_multi': 4.865151e-07, 'Disease': 'AD', 'b_SMR': 0.0212427, 'p_HEIDI': 0.001081871}]
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SMR Significance, Effect
Q40.342
Q40
Are there any specific alleles within the gene RP11-293E1.1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene RP11-293E1.1 that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs111327992 • Prefrontal Cortex: Adjusted SMR multi-SNP P-value: 1.76e-06; b: 9.3036e-01
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-293E1.1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1242270', 'Gene': 'RP11-293E1.1', 'Omic_tissue': 'Prefrontal Cortex', 'topSNP': 'rs111327992', 'A1': 'A', 'A2': 'G', 'Freq': 0.236196, 'p_SMR_multi': 1.757393e-06, 'Disease': 'PD', 'b_SMR': 0.930361, 'p_HEIDI': -9999.0}]
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SMR Significance, Effect
Q40.1198
Q40
Are there any specific alleles within the gene ATP10D associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Cortex, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene ATP10D that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ATP10D' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.29
Q40
Are there any specific alleles within the gene LRRC37A2 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
Yes, there are 6 alleles within the gene LRRC37A2 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy: • rs169201 • Whole Blood: Adjusted SMR multi-SNP P-value: 3.86e-44; b: 1.6819e+00 • Whole Brain: Adjusted SMR multi-SNP P-value: 1.45e-32; b: 1.1838e...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'LRRC37A2' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1579429', 'Gene': 'LRRC37A2', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs169201', 'A1': 'G', 'A2': 'A', 'Freq': 0.219836, 'p_SMR_multi': 3.8561219999999997e-44, 'Disease': 'PSP', 'b_SMR': 1.6819, 'p_HEIDI': 1.459323e-11}, {'UUID': 'NDD_SMR_genes_all_update_text_1154400', 'Gene':...
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Q40.1227
Q40
Are there any specific alleles within the gene AC091132.1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene AC091132.1 that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs1724400 • Cerebellum: Adjusted SMR multi-SNP P-value: 6.17e-08; b: 3.5712e-01
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'AC091132.1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1710341', 'Gene': 'AC091132.1', 'Omic_tissue': 'Cerebellum', 'topSNP': 'rs1724400', 'A1': 'C', 'A2': 'A', 'Freq': 0.738241, 'p_SMR_multi': 6.167256e-08, 'Disease': 'PD', 'b_SMR': 0.357115, 'p_HEIDI': 0.116595}]
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Q40.1434
Q40
Are there any specific alleles within the gene SOAT1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain and Nucleus Accumbens Basal samples tested, there are no alleles within the gene SOAT1 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SOAT1' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1954
Q40
Are there any specific alleles within the gene ZNF646 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene ZNF646 that are significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs7294 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.78e-07; b: 1.5994e-01 • rs4889530 • Multi Ancestry Whole Brain: Adjusted SMR multi-SNP P-value: 9.95e-07...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ZNF646' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_974687', 'Gene': 'ZNF646', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs7294', 'A1': 'T', 'A2': 'C', 'Freq': 0.365031, 'p_SMR_multi': 2.778268e-07, 'Disease': 'PD', 'b_SMR': 0.159944, 'p_HEIDI': 2.023725e-05}, {'UUID': 'NDD_SMR_genes_all_update_text_1435346', 'Gene': 'ZNF646', 'Om...
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Q40.954
Q40
Are there any specific alleles within the gene RP11-1109M24.8 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene RP11-1109M24.8 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-1109M24.8' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.172
Q40
Are there any specific alleles within the gene NEIL3 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene NEIL3 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'NEIL3' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1406
Q40
Are there any specific alleles within the gene TAS1R1 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene TAS1R1 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'TAS1R1' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1207
Q40
Are there any specific alleles within the gene SCFD1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene SCFD1 that is significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis: • rs229243 • Multi Ancestry Whole Brain: Adjusted SMR multi-SNP P-value: 2.95e-06; b: 1.2198e-01
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SCFD1' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1405224', 'Gene': 'SCFD1', 'Omic_tissue': 'Multi Ancestry Whole Brain', 'topSNP': 'rs229243', 'A1': 'A', 'A2': 'C', 'Freq': 0.354806, 'p_SMR_multi': 2.949612e-06, 'Disease': 'ALS', 'b_SMR': 0.12198, 'p_HEIDI': 0.000337994}]
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SMR Significance, Effect
Q40.1263
Q40
Are there any specific alleles within the gene MYL1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Skeletal Muscle samples tested, there are no alleles within the gene MYL1 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'MYL1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1400
Q40
Are there any specific alleles within the gene RP4-665J23.2 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RP4-665J23.2 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP4-665J23.2' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.920
Q40
Are there any specific alleles within the gene MAPT associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there are 17 alleles within the gene MAPT that are significantly associated with an increased susceptibility to developing Parkinson's Disease. Here are the top 10: • rs570200944 • Prefrontal Cortex: Adjusted SMR multi-SNP P-value: 9.25e-16; b: 5.7434e-01 • rs62063271 • Whole Blood: Adjusted SMR multi-SNP ...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'MAPT' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1242273', 'Gene': 'MAPT', 'Omic_tissue': 'Prefrontal Cortex', 'topSNP': 'rs570200944', 'A1': 'A', 'A2': 'G', 'Freq': 0.236196, 'p_SMR_multi': 9.246003e-16, 'Disease': 'PD', 'b_SMR': 0.574337, 'p_HEIDI': 0.002694627}, {'UUID': 'NDD_SMR_genes_all_update_text_948891', 'Gene': 'MAPT...
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SMR Significance, Effect
Q40.497
Q40
Are there any specific alleles within the gene TBCK associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene TBCK that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'TBCK' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.962
Q40
Are there any specific alleles within the gene CFAP97D2 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cortex samples tested, there are no alleles within the gene CFAP97D2 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CFAP97D2' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1106
Q40
Are there any specific alleles within the gene RP11-343N15.5 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RP11-343N15.5 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-343N15.5' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Q40.1041
Q40
Are there any specific alleles within the gene RP11-136K7.2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex and Liver samples tested, there are no alleles within the gene RP11-136K7.2 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-136K7.2' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.594
Q40
Are there any specific alleles within the gene GPR123 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Prefrontal Cortex and Liver samples tested, there are no alleles within the gene GPR123 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'GPR123' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.757
Q40
Are there any specific alleles within the gene UTP11L associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene UTP11L that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'UTP11L' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[]
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SMR Significance, Effect
Q40.664
Q40
Are there any specific alleles within the gene LINC00311 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene LINC00311 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'LINC00311' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.237
Q40
Are there any specific alleles within the gene RP4-559A3.7 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene RP4-559A3.7 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP4-559A3.7' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.739
Q40
Are there any specific alleles within the gene ST3GAL6 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene ST3GAL6 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ST3GAL6' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[]
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SMR Significance, Effect
Q40.1989
Q40
Are there any specific alleles within the gene RPS18P9 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Tibial Nerve, Multi Ancestry Whole Brain, Whole Blood and Cerebellum samples tested, there are no alleles within the gene RPS18P9 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RPS18P9' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1633
Q40
Are there any specific alleles within the gene GDPGP1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene GDPGP1 that are significantly associated with an increased susceptibility to developing Lewy Body Dement...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'GDPGP1' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1166
Q40
Are there any specific alleles within the gene PCDHA1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cerebellar Hemisphere and Cerebellum samples tested, there are no alleles within the gene PCDHA1 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'PCDHA1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1471
Q40
Are there any specific alleles within the gene LRRC32 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene LRRC32 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'LRRC32' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1913
Q40
Are there any specific alleles within the gene RP11-159D23.2 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RP11-159D23.2 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-159D23.2' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1628
Q40
Are there any specific alleles within the gene TMEM204 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Tibial Nerve and Whole Blood samples tested, there are no alleles within the gene TMEM204 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'TMEM204' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.943
Q40
Are there any specific alleles within the gene APOC2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 9 alleles within the gene APOC2 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs5120 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.28e-24; b: 6.1811e-02 • rs7252480 • Whole Blood: Adjusted SMR multi-SNP P-value: 4.74e-11; b: 1.4504e-01 ...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'APOC2' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_637437', 'Gene': 'APOC2', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs5120', 'A1': 'T', 'A2': 'A', 'Freq': 0.514315, 'p_SMR_multi': 1.276397e-24, 'Disease': 'AD', 'b_SMR': 0.0618107, 'p_HEIDI': 2.572368e-19}, {'UUID': 'NDD_SMR_genes_all_update_text_637436', 'Gene': 'APOC2', 'Omic...
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SMR Significance, Effect
Q40.1219
Q40
Are there any specific alleles within the gene WDR11 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Basal Ganglia, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Hypothalamus, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala, Whole Brain and Nucleus...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'WDR11' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1074
Q40
Are there any specific alleles within the gene MR1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Cortex, Prefrontal Cortex, Tibial Nerve, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene MR1 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'MR1' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.111
Q40
Are there any specific alleles within the gene NAT16 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex and Caudate Basal Ganglia samples tested, there are no alleles within the gene NAT16 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'NAT16' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1944
Q40
Are there any specific alleles within the gene SLC25A13 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cerebellar Hemisphere and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene SLC25A13 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SLC25A13' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.574
Q40
Are there any specific alleles within the gene RP11-707O23.5 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene RP11-707O23.5 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs62066086 • Whole Brain: Adjusted SMR multi-SNP P-value: 2.93e-06; b: 6.3220e-02
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-707O23.5' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_115147', 'Gene': 'RP11-707O23.5', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs62066086', 'A1': 'G', 'A2': 'A', 'Freq': 0.236196, 'p_SMR_multi': 2.932925e-06, 'Disease': 'AD', 'b_SMR': 0.06322, 'p_HEIDI': -9999.0}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1177
Q40
Are there any specific alleles within the gene UGCG associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene UGCG that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'UGCG' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1184
Q40
Are there any specific alleles within the gene ABCA4 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Cortex samples tested, there are no alleles within the gene ABCA4 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ABCA4' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.897
Q40
Are there any specific alleles within the gene PPHLN1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cerebellar Hemisphere, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene PPHLN1 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'PPHLN1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.956
Q40
Are there any specific alleles within the gene CTD-2139B15.2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene CTD-2139B15.2 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CTD-2139B15.2' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1057
Q40
Are there any specific alleles within the gene RP11-492E3.51 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RP11-492E3.51 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-492E3.51' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1354
Q40
Are there any specific alleles within the gene GFM1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Substantia nigra and Anterior Cingulate Cortex BA24 samples tested, there are no alleles within the gene GFM1 that are significantly associated...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'GFM1' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1373
Q40
Are there any specific alleles within the gene MIR376A1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene MIR376A1 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'MIR376A1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1448
Q40
Are there any specific alleles within the gene YTHDF1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene YTHDF1 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'YTHDF1' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.891
Q40
Are there any specific alleles within the gene AC004623.2 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene AC004623.2 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'AC004623.2' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1673
Q40
Are there any specific alleles within the gene SETD1A associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene SETD1A that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs11150601 • Whole Brain: Adjusted SMR multi-SNP P-value: 3.40e-07; b: 2.5722e-01
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SETD1A' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_485446', 'Gene': 'SETD1A', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs11150601', 'A1': 'G', 'A2': 'A', 'Freq': 0.361963, 'p_SMR_multi': 3.404339e-07, 'Disease': 'PD', 'b_SMR': 0.257218, 'p_HEIDI': 8.535299e-05}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.857
Q40
Are there any specific alleles within the gene CREG1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene CREG1 that are significantly associated with an increased susceptibility to developing L...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CREG1' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.741
Q40
Are there any specific alleles within the gene LNP1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene LNP1 ...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'LNP1' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.724
Q40
Are there any specific alleles within the gene AC093391.2 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene AC093391.2 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'AC093391.2' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.460
Q40
Are there any specific alleles within the gene RNF5P1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RNF5P1 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RNF5P1' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.267
Q40
Are there any specific alleles within the gene AC016735.1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene AC016735.1 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'AC016735.1' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.78
Q40
Are there any specific alleles within the gene SLC11A1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene SLC11A1 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SLC11A1' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1785
Q40
Are there any specific alleles within the gene LRPPRC associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Substantia nigra, Hypothalamus, Anterior Cingulate Cortex BA24, Whole Blood, Putamen Basal Ganglia, Amygdala and Nucl...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'LRPPRC' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.450
Q40
Are there any specific alleles within the gene CCNE2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene CCNE2 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs2515226 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.50e-06; b: 5.4211e-01
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CCNE2' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1496487', 'Gene': 'CCNE2', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs2515226', 'A1': 'A', 'A2': 'G', 'Freq': 0.360941, 'p_SMR_multi': 2.499329e-06, 'Disease': 'AD', 'b_SMR': 0.542112, 'p_HEIDI': 0.2756845}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.401
Q40
Are there any specific alleles within the gene SIPA1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene SIPA1 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SIPA1' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.179
Q40
Are there any specific alleles within the gene RP11-422P24.10 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex samples tested, there are no alleles within the gene RP11-422P24.10 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-422P24.10' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1051
Q40
Are there any specific alleles within the gene TRGV4 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex, Tibial Nerve, Substantia nigra, Liver and Whole Blood samples tested, there are no alleles within the gene TRGV4 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'TRGV4' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1737
Q40
Are there any specific alleles within the gene PLD2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene PLD2 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs2286670 • Whole Blood: Adjusted SMR multi-SNP P-value: 5.05e-08; b: 9.5071e-02
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'PLD2' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1501909', 'Gene': 'PLD2', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs2286670', 'A1': 'T', 'A2': 'G', 'Freq': 0.162577, 'p_SMR_multi': 5.045019e-08, 'Disease': 'AD', 'b_SMR': 0.0950705, 'p_HEIDI': 0.004146128}]
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SMR Significance, Effect
Q40.1609
Q40
Are there any specific alleles within the gene KAT8 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there are 4 alleles within the gene KAT8 that are significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs4527034 • Multi Ancestry Whole Brain: Adjusted SMR multi-SNP P-value: 1.02e-08; b: 1.3102e-01 • rs1978487 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.53e-0...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'KAT8' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1435348', 'Gene': 'KAT8', 'Omic_tissue': 'Multi Ancestry Whole Brain', 'topSNP': 'rs4527034', 'A1': 'A', 'A2': 'G', 'Freq': 0.380368, 'p_SMR_multi': 1.024732e-08, 'Disease': 'PD', 'b_SMR': 0.131023, 'p_HEIDI': 1.064305e-10}, {'UUID': 'NDD_SMR_genes_all_update_text_974691', 'Gene...
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SMR Significance, Effect
Q40.1869
Q40
Are there any specific alleles within the gene DSCR4 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene DSCR4 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'DSCR4' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.602
Q40
Are there any specific alleles within the gene IGSF21 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Cerebellar Hemisphere and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene IGSF21 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'IGSF21' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.63
Q40
Are there any specific alleles within the gene MRPL41 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Tibial Nerve, Multi Ancestry Whole Brain, Liver and Cerebellum samples tested, there are no alleles within the gene MRPL41 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'MRPL41' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1309
Q40
Are there any specific alleles within the gene ZFP57 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene ZFP57 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs2747429 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.31e-06; b: 2.1058e-02
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ZFP57' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_619934', 'Gene': 'ZFP57', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs2747429', 'A1': 'C', 'A2': 'T', 'Freq': 0.185072, 'p_SMR_multi': 2.309027e-06, 'Disease': 'AD', 'b_SMR': 0.0210576, 'p_HEIDI': 0.2518906}]
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SMR Significance, Effect
Q40.879
Q40
Are there any specific alleles within the gene SLC25A39P2 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Prefrontal Cortex samples tested, there are no alleles within the gene SLC25A39P2 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SLC25A39P2' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1491
Q40
Are there any specific alleles within the gene TTC3 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Hypothalamus, Liver, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alle...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'TTC3' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1880
Q40
Are there any specific alleles within the gene SOCS5P2 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Anterior Cingulate Cortex BA24 samples tested, there are no alleles within the gene SOCS5P2 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SOCS5P2' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.282
Q40
Are there any specific alleles within the gene SPOPL associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene SPOPL that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SPOPL' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.37
Q40
Are there any specific alleles within the gene FGD6 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene FGD6 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'FGD6' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1517
Q40
Are there any specific alleles within the gene ACO1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Skeletal Muscle, Multi Ancestry Whole Brain and Nucleus Accumbens Basal samples tested, there are no alleles within the gene ACO1 that are significantly associated with an increased susceptibi...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ACO1' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.669
Q40
Are there any specific alleles within the gene NDUFAF3 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene NDUFAF3 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'NDUFAF3' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1829
Q40
Are there any specific alleles within the gene RP11-1167A19.2 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RP11-1167A19.2 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-1167A19.2' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1446
Q40
Are there any specific alleles within the gene MRPL20 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Cortex, Frontal Cortex, Cerebellar Hemisphere, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Substantia nigra, Hypothalamus, Liver, Anterior Cingulate Cortex BA24, Whole Blood, Putamen Basal Ganglia, Whole Brain and Nucleus Accumbens Basal sa...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'MRPL20' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.986
Q40
Are there any specific alleles within the gene ARSG associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene ARSG that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ARSG' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1572
Q40
Are there any specific alleles within the gene AP2B1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex, Skeletal Muscle, Multi Ancestry Whole Brain, Putamen Basal Ganglia and Amygdala samples tested, there are no alleles within the gene AP2B1 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'AP2B1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.745
Q40
Are there any specific alleles within the gene SMARCAL1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Cortex, Prefrontal Cortex, Tibial Nerve, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene SMARCAL1 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SMARCAL1' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.194
Q40
Are there any specific alleles within the gene AP000679.2 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain and Whole Blood samples tested, there are no alleles within the gene AP000679.2 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'AP000679.2' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.927
Q40
Are there any specific alleles within the gene GAPDHP48 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex samples tested, there are no alleles within the gene GAPDHP48 that are significantly associated with an increased susceptibility to developing Lewy Body Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'GAPDHP48' AND Disease = 'LBD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.462
Q40
Are there any specific alleles within the gene POU5F1P6 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Blood, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Cortex, Hippocampus, Whole Brain and Cerebellum samples tested, there are no alleles within the gene POU5F1P6 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'POU5F1P6' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.682
Q40
Are there any specific alleles within the gene RP5-1052I5.1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Substantia nigra, Liver, Putamen Basal Ganglia, Cerebellum and Nucleus Accumbens Basal samples tested, there are no alleles within the gene RP5-1052I5.1 that are significantly associated with an increased susceptibility to developing Park...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP5-1052I5.1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.767
Q40
Are there any specific alleles within the gene PVR associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene PVR that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs79572806 • Whole Blood: Adjusted SMR multi-SNP P-value: 7.20e-09; b: 1.8058e-01
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'PVR' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1503902', 'Gene': 'PVR', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs79572806', 'A1': 'T', 'A2': 'C', 'Freq': 0.0889571, 'p_SMR_multi': 7.19757e-09, 'Disease': 'AD', 'b_SMR': 0.180575, 'p_HEIDI': 6.987784e-08}]
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SMR Significance, Effect
Q40.1809
Q40
Are there any specific alleles within the gene TSSK6 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene TSSK6 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'TSSK6' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1603
Q40
Are there any specific alleles within the gene ZNF503 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cerebellum, Cortex, Cerebellar Hemisphere, Multi Ancestry Whole Brain, Whole Blood and Whole Brain samples tested, there are no alleles within the gene ZNF503 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ZNF503' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.735
Q40
Are there any specific alleles within the gene UBOX5 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain and Nucleus Accumbens Basal samples tested, there are no alleles within the gene UBOX5 that are significantly associated with an increased susceptibility to ...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'UBOX5' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.418
Q40
Are there any specific alleles within the gene CFL2 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Tibial Nerve samples tested, there are no alleles within the gene CFL2 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CFL2' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1107
Q40
Are there any specific alleles within the gene C4orf47 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood and Cortex samples tested, there are no alleles within the gene C4orf47 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'C4orf47' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.832
Q40
Are there any specific alleles within the gene RP13-735L24.1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Liver, Whole Blood, Whole Brain and Cerebellum samples tested, there are no alleles within the gene RP13-735L24.1 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP13-735L24.1' AND Disease = 'FTD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1498
Q40
Are there any specific alleles within the gene ACP7 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cerebellum and Cortex samples tested, there are no alleles within the gene ACP7 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ACP7' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.623
Q40
Are there any specific alleles within the gene TSBP1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene TSBP1 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs9469094 • Cortex: Adjusted SMR multi-SNP P-value: 4.21e-08; b: 5.8905e-03
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'TSBP1' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_1109082', 'Gene': 'TSBP1', 'Omic_tissue': 'Cortex', 'topSNP': '6:32255414:rs9469094:G_C', 'A1': 'G', 'A2': 'C', 'Freq': 0.969325, 'p_SMR_multi': 4.212407e-08, 'Disease': 'AD', 'b_SMR': 0.00589053, 'p_HEIDI': 0.4811921}]
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SMR Significance, Effect
Q40.117
Q40
Are there any specific alleles within the gene ACKR1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cortex samples tested, there are no alleles within the gene ACKR1 that are significantly associated with an increased susceptibility to developing Parkinson's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ACKR1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.423
Q40
Are there any specific alleles within the gene RHOT1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Prefrontal Cortex, Tibial Nerve, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene RHOT1 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RHOT1' AND Disease = 'AD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect
Q40.1911
Q40
Are there any specific alleles within the gene ASS1P1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene ASS1P1 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral Sclerosis.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ASS1P1' AND Disease = 'ALS' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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SMR Significance, Effect