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Q40.1408
Q40
Are there any specific alleles within the gene PLVAP associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene PLVAP 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 = 'PLVAP' 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
Q40.806
Q40
Are there any specific alleles within the gene AGFG2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene AGFG2 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs2734897 • Cerebellum: Adjusted SMR multi-SNP P-value: 7.44e-08; b: 1.4750e-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 = 'AGFG2' 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_1687938', 'Gene': 'AGFG2', 'Omic_tissue': 'Cerebellum', 'topSNP': 'rs2734897', 'A1': 'G', 'A2': 'A', 'Freq': 0.695297, 'p_SMR_multi': 7.442622e-08, 'Disease': 'AD', 'b_SMR': 0.147502, 'p_HEIDI': 0.2152247}]
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SMR Significance, Effect
Q40.1067
Q40
Are there any specific alleles within the gene C12orf70 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 C12orf70 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 = 'C12orf70' 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
Q40.622
Q40
Are there any specific alleles within the gene POLR2E associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 4 alleles within the gene POLR2E that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs6843 • Multi Ancestry Whole Brain: Adjusted SMR multi-SNP P-value: 5.17e-10; b: 5.6446e-02 • rs2238586 • Cortex: Adjusted SMR multi-SNP P-value: 4.06e-09; b: ...
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 = 'POLR2E' 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_1397183', 'Gene': 'POLR2E', 'Omic_tissue': 'Multi Ancestry Whole Brain', 'topSNP': 'rs6843', 'A1': 'T', 'A2': 'C', 'Freq': 0.243354, 'p_SMR_multi': 5.172203e-10, 'Disease': 'AD', 'b_SMR': 0.0564458, 'p_HEIDI': 0.0001171661}, {'UUID': 'NDD_SMR_genes_all_update_text_1107634', 'Gen...
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SMR Significance, Effect
Q40.298
Q40
Are there any specific alleles within the gene NEURL3 associated with increased susceptibility to developing Parkinson's Disease, 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 NEURL3 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 = 'NEURL3' 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
Q40.912
Q40
Are there any specific alleles within the gene MAMSTR associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Caudate Basal Ganglia, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Hypothalamus, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene MAMSTR that are significantly associated with an increased susceptibili...
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 = 'MAMSTR' 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
Q40.917
Q40
Are there any specific alleles within the gene LINC00368 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere samples tested, there are no alleles within the gene LINC00368 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 = 'LINC00368' 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
Q40.1903
Q40
Are there any specific alleles within the gene RBM22 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 RBM22 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 = 'RBM22' 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
Q40.91
Q40
Are there any specific alleles within the gene RP11-573D15.9 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Prefrontal Cortex and Whole Blood samples tested, there are no alleles within the gene RP11-573D15.9 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 = 'RP11-573D15.9' 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
Q40.42
Q40
Are there any specific alleles within the gene VN1R82P 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 VN1R82P 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 = 'VN1R82P' 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
Q40.1803
Q40
Are there any specific alleles within the gene MTMR2 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene MTMR2 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 = 'MTMR2' 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
Q40.1934
Q40
Are there any specific alleles within the gene SMIM15 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 SMIM15 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 = 'SMIM15' 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
Q40.134
Q40
Are there any specific alleles within the gene RP3-512B11.3 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Tibial Nerve and Liver samples tested, there are no alleles within the gene RP3-512B11.3 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 = 'RP3-512B11.3' 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
Q40.1566
Q40
Are there any specific alleles within the gene CTD-3018O17.3 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Prefrontal Cortex, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene CTD-3018O17.3 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-3018O17.3' 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
Q40.977
Q40
Are there any specific alleles within the gene LAMB2 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 LAMB2 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 = 'LAMB2' 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
Q40.1070
Q40
Are there any specific alleles within the gene RP11-428J1.4 associated with increased susceptibility to developing Alzheimer's Disease, 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 RP11-428J1.4 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 = 'RP11-428J1.4' 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
Q40.1856
Q40
Are there any specific alleles within the gene PLAAT1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cortex samples tested, there are no alleles within the gene PLAAT1 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 = 'PLAAT1' 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
Q40.1346
Q40
Are there any specific alleles within the gene GRN associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene GRN that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs5848 • Multi Ancestry Whole Brain: Adjusted SMR multi-SNP P-value: 3.18e-07; b: 1.3019e-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 = 'GRN' 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_1396727', 'Gene': 'GRN', 'Omic_tissue': 'Multi Ancestry Whole Brain', 'topSNP': 'rs5848', 'A1': 'T', 'A2': 'C', 'Freq': 0.304703, 'p_SMR_multi': 3.175137e-07, 'Disease': 'AD', 'b_SMR': 0.130186, 'p_HEIDI': 0.0003317978}]
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SMR Significance, Effect
Q40.1831
Q40
Are there any specific alleles within the gene AC024560.3 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Substantia nigra, Hypothalamus, Putamen Basal Ganglia, Cerebellum and Nucleus Accumbens Basal samples tested, there ...
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 = 'AC024560.3' 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
Q40.167
Q40
Are there any specific alleles within the gene CAPN9 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Basal Ganglia, Hippocampus, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Substantia nigra, Hypothalamus, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala and Nucleus Accumbens Basal samples tested, ...
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 = 'CAPN9' 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
Q40.731
Q40
Are there any specific alleles within the gene KPNA1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Caudate Basal Ganglia, Multi Ancestry Whole Brain, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene KPNA1 that are significantly associated with an increased susceptibility to d...
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 = 'KPNA1' 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
Q40.294
Q40
Are there any specific alleles within the gene TAS2R63P associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve and Cerebellum samples tested, there are no alleles within the gene TAS2R63P 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 = 'TAS2R63P' 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
Q40.1142
Q40
Are there any specific alleles within the gene SMCR7 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 SMCR7 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 = 'SMCR7' 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
Q40.1536
Q40
Are there any specific alleles within the gene DDX20 associated with increased susceptibility to developing Progressive supranuclear palsy, 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 DDX20 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 = 'DDX20' 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
Q40.1897
Q40
Are there any specific alleles within the gene ZNF219 associated with increased susceptibility to developing Alzheimer's Disease, 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 ZNF219 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 = 'ZNF219' 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
Q40.1006
Q40
Are there any specific alleles within the gene TNNI1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood and Liver samples tested, there are no alleles within the gene TNNI1 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 = 'TNNI1' 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
Q40.1421
Q40
Are there any specific alleles within the gene POLK associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Blood, Cerebellar Hemisphere, Tibial Nerve, Multi Ancestry Whole Brain and Whole Brain samples tested, there are no alleles within the gene POLK 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 = 'POLK' 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
Q40.785
Q40
Are there any specific alleles within the gene SLC25A27 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Basal Ganglia, Hippocampus, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Substantia nigra, Hypothalamus, Liver, Anterior Cingulate Cortex BA24, Putamen Basal Gang...
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 = 'SLC25A27' 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
Q40.846
Q40
Are there any specific alleles within the gene CTB-58E17.3 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 CTB-58E17.3 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 = 'CTB-58E17.3' 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
Q40.352
Q40
Are there any specific alleles within the gene CTTNBP2NL associated with increased susceptibility to developing Progressive supranuclear palsy, 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 CTTNBP2NL 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 = 'CTTNBP2NL' 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
Q40.1945
Q40
Are there any specific alleles within the gene RP5-1042K10.12 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 RP5-1042K10.12 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 = 'RP5-1042K10.12' 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
Q40.577
Q40
Are there any specific alleles within the gene C4orf21 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Frontal Cortex, Prefrontal Cortex, Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Liver, Putamen Basal Ganglia, Amygdala, Whole Brain, Cerebellum and Nucleus Accumbens Basal samples tested, there are no alleles within the gene C4orf21 that are significantly associated w...
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 = 'C4orf21' 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
Q40.1923
Q40
Are there any specific alleles within the gene BCL7C associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene BCL7C 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 = 'BCL7C' 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
Q40.1888
Q40
Are there any specific alleles within the gene CRYBB3 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Liver, Anterior Cingulate Cortex BA24, Whole Brain and Nucleus Accumbens Basal samples tested, there are no alleles within the gene CRYBB3 that are significantly associated with an increased susceptibility to developing Frontote...
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 = 'CRYBB3' 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
Q40.1470
Q40
Are there any specific alleles within the gene LINC00200 associated with increased susceptibility to developing Lewy Body 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 LINC00200 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 = 'LINC00200' 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
Q40.1818
Q40
Are there any specific alleles within the gene FAM131B associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene FAM131B that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs13232480 • Whole Blood: Adjusted SMR multi-SNP P-value: 8.03e-07; b: 2.2714e-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 = 'FAM131B' 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_1496068', 'Gene': 'FAM131B', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs13232480', 'A1': 'T', 'A2': 'C', 'Freq': 0.182004, 'p_SMR_multi': 8.029512e-07, 'Disease': 'AD', 'b_SMR': 0.0227139, 'p_HEIDI': 0.07492317}]
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SMR Significance, Effect
Q40.1317
Q40
Are there any specific alleles within the gene ARL17B associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there are 3 alleles within the gene ARL17B that are significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs151267673 • Prefrontal Cortex: Adjusted SMR multi-SNP P-value: 5.99e-08; b: 1.1585e-01 • rs17698176 • Skeletal Muscle: Adjusted SMR multi-SNP P-value: 8.33e-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 = 'ARL17B' 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_1242283', 'Gene': 'ARL17B', 'Omic_tissue': 'Prefrontal Cortex', 'topSNP': 'rs151267673', 'A1': 'A', 'A2': 'C', 'Freq': 0.747444, 'p_SMR_multi': 5.993072e-08, 'Disease': 'PD', 'b_SMR': 0.115846, 'p_HEIDI': 2.382316e-07}, {'UUID': 'NDD_SMR_genes_all_update_text_1370549', 'Gene': '...
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SMR Significance, Effect
Q40.1501
Q40
Are there any specific alleles within the gene EIF2B2 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Basal Ganglia, Spinalcord, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Hypothalamus, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia and Amygdala samples tested, there are no alleles within ...
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 = 'EIF2B2' 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
Q40.464
Q40
Are there any specific alleles within the gene AF127936.7 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 AF127936.7 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 = 'AF127936.7' 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
Q40.381
Q40
Are there any specific alleles within the gene FMC1 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 FMC1 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 = 'FMC1' 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
Q40.1344
Q40
Are there any specific alleles within the gene SOX9-AS1 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 SOX9-AS1 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 = 'SOX9-AS1' 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
Q40.337
Q40
Are there any specific alleles within the gene DENND2C associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene DENND2C 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 = 'DENND2C' 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
Q40.1284
Q40
Are there any specific alleles within the gene RP11-342M1.7 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 RP11-342M1.7 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 = 'RP11-342M1.7' 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
Q40.1762
Q40
Are there any specific alleles within the gene ANKRD66 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain and Cortex samples tested, there are no alleles within the gene ANKRD66 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 = 'ANKRD66' 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
Q40.1459
Q40
Are there any specific alleles within the gene KCNN3 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene KCNN3 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 = 'KCNN3' 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
Q40.823
Q40
Are there any specific alleles within the gene BIN1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 8 alleles within the gene BIN1 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs11682128 • Whole Blood: Adjusted SMR multi-SNP P-value: 4.63e-38; b: 1.3694e-01 • rs6720234 • Whole Blood: Adjusted SMR multi-SNP P-value: 5.82e-18; b: 8.5200e-...
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 = 'BIN1' 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_1491965', 'Gene': 'BIN1', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs11682128', 'A1': 'A', 'A2': 'G', 'Freq': 0.357873, 'p_SMR_multi': 4.6304359999999996e-38, 'Disease': 'AD', 'b_SMR': 0.13694, 'p_HEIDI': 1.531931e-10}, {'UUID': 'NDD_SMR_genes_all_update_text_631125', 'Gene': 'B...
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SMR Significance, Effect
Q40.1114
Q40
Are there any specific alleles within the gene BUD13 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 BUD13 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 = 'BUD13' 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
Q40.1524
Q40
Are there any specific alleles within the gene LIFR-AS1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene LIFR-AS1 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 = 'LIFR-AS1' 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
Q40.1941
Q40
Are there any specific alleles within the gene AC118754.4 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 AC118754.4 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 = 'AC118754.4' 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
Q40.1616
Q40
Are there any specific alleles within the gene CNN2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene CNN2 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs113337161 • Whole Blood: Adjusted SMR multi-SNP P-value: 3.83e-14; b: 1.1211e-01 • rs3087680 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.39e-06; b: 1.2246e...
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 = 'CNN2' 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_1503131', 'Gene': 'CNN2', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs113337161', 'A1': 'T', 'A2': 'C', 'Freq': 0.0858896, 'p_SMR_multi': 3.829816e-14, 'Disease': 'AD', 'b_SMR': 0.112112, 'p_HEIDI': 8.598535e-10}, {'UUID': 'NDD_SMR_genes_all_update_text_1652807', 'Gene': 'CNN2', ...
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SMR Significance, Effect
Q40.1898
Q40
Are there any specific alleles within the gene C15orf54 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 C15orf54 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 = 'C15orf54' 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
Q40.918
Q40
Are there any specific alleles within the gene RFPL1-AS1 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 RFPL1-AS1 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 = 'RFPL1-AS1' 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
Q40.1930
Q40
Are there any specific alleles within the gene RP11-32K4.1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RP11-32K4.1 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 = 'RP11-32K4.1' 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
Q40.1126
Q40
Are there any specific alleles within the gene ITGAX associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene ITGAX that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs11574631 • Whole Blood: Adjusted SMR multi-SNP P-value: 3.17e-08; b: 3.6051e-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 = 'ITGAX' 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_1501486', 'Gene': 'ITGAX', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs11574631', 'A1': 'C', 'A2': 'T', 'Freq': 0.315951, 'p_SMR_multi': 3.173201e-08, 'Disease': 'AD', 'b_SMR': 0.0360512, 'p_HEIDI': 0.0003262819}]
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SMR Significance, Effect
Q40.332
Q40
Are there any specific alleles within the gene SEBOX associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cortex samples tested, there are no alleles within the gene SEBOX 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 = 'SEBOX' 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
Q40.1036
Q40
Are there any specific alleles within the gene RP11-325D8.1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Tibial Nerve samples tested, there are no alleles within the gene RP11-325D8.1 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 = 'RP11-325D8.1' 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
Q40.322
Q40
Are there any specific alleles within the gene RP11-644F5.11 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene RP11-644F5.11 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 = 'RP11-644F5.11' 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
Q40.1531
Q40
Are there any specific alleles within the gene ATP5G1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Blood, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Whole Brain and Cerebellum samples tested, there are no alleles within the gene ATP5G1 that are significantly associated with an increased susceptibility to developi...
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 = 'ATP5G1' 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
Q40.1360
Q40
Are there any specific alleles within the gene RP11-439E19.7 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Frontal Cortex, Cortex, Skeletal Muscle and Putamen Basal Ganglia samples tested, there are no alleles within the gene RP11-439E19.7 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 = 'RP11-439E19.7' 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
Q40.1734
Q40
Are there any specific alleles within the gene TEX37 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 TEX37 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 = 'TEX37' 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
Q40.170
Q40
Are there any specific alleles within the gene TREML2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene TREML2 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs2006080 • Whole Brain: Adjusted SMR multi-SNP P-value: 2.08e-06; b: 1.9007e-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 = 'TREML2' 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_67042', 'Gene': 'TREML2', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs2006080', 'A1': 'C', 'A2': 'T', 'Freq': 0.834356, 'p_SMR_multi': 2.079623e-06, 'Disease': 'AD', 'b_SMR': 0.0190074, 'p_HEIDI': 1.158931e-05}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.13
Q40
Are there any specific alleles within the gene MAD2L2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Multi Ancestry Whole Brain and Cerebellum samples tested, there are no alleles within the gene MAD2L2 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 = 'MAD2L2' 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
Q40.1927
Q40
Are there any specific alleles within the gene GABRA5 associated with increased susceptibility to developing Frontotemporal 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 GABRA5 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 = 'GABRA5' 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
Q40.174
Q40
Are there any specific alleles within the gene CTA-384D8.35 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene CTA-384D8.35 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 = 'CTA-384D8.35' 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
Q40.656
Q40
Are there any specific alleles within the gene CDSN associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene CDSN that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs1042148 • Whole Blood: Adjusted SMR multi-SNP P-value: 3.52e-07; b: 2.2286e-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 = 'CDSN' 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_620705', 'Gene': 'CDSN', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs1042148', 'A1': 'T', 'A2': 'C', 'Freq': 0.266871, 'p_SMR_multi': 3.519033e-07, 'Disease': 'AD', 'b_SMR': 0.022286, 'p_HEIDI': 0.03739201}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1062
Q40
Are there any specific alleles within the gene CORO6 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, Multi Ancestry Whole Brain and Cerebellum samples tested, there are no alleles within the gene CORO6 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 = 'CORO6' 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
Q40.263
Q40
Are there any specific alleles within the gene AC092684.1 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 AC092684.1 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 = 'AC092684.1' 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
Q40.1427
Q40
Are there any specific alleles within the gene RP4-734P14.4 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 RP4-734P14.4 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 = 'RP4-734P14.4' 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
Q40.1582
Q40
Are there any specific alleles within the gene AC012454.4 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 AC012454.4 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 = 'AC012454.4' 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
Q40.909
Q40
Are there any specific alleles within the gene DLK1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Skeletal Muscle samples tested, there are no alleles within the gene DLK1 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 = 'DLK1' 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
Q40.679
Q40
Are there any specific alleles within the gene CASTOR3 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene CASTOR3 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs17309333 • Cortex: Adjusted SMR multi-SNP P-value: 1.21e-06; b: 9.2866e-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 = 'CASTOR3' 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_1105974', 'Gene': 'CASTOR3', 'Omic_tissue': 'Cortex', 'topSNP': '7:100215469:rs17309333:C_A', 'A1': 'C', 'A2': 'A', 'Freq': 0.958078, 'p_SMR_multi': 1.214914e-06, 'Disease': 'AD', 'b_SMR': 0.00928661, 'p_HEIDI': 0.5580988}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.261
Q40
Are there any specific alleles within the gene FAM180B 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, Prefrontal Cortex and Nucleus Accumbens Basal samples tested, there are no alleles within the gene FAM180B 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 = 'FAM180B' 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
Q40.851
Q40
Are there any specific alleles within the gene SCUBE3 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, 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 SCUBE3 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 = 'SCUBE3' 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
Q40.874
Q40
Are there any specific alleles within the gene PRSS36 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene PRSS36 that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs55667375 • Whole Brain: Adjusted SMR multi-SNP P-value: 2.18e-06; b: 1.3737e-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 = 'PRSS36' 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_485473', 'Gene': 'PRSS36', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs55667375', 'A1': 'C', 'A2': 'T', 'Freq': 0.710634, 'p_SMR_multi': 2.181694e-06, 'Disease': 'PD', 'b_SMR': 0.137373, 'p_HEIDI': 0.1779642}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1564
Q40
Are there any specific alleles within the gene RP11-338C15.3 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Blood samples tested, there are no alleles within the gene RP11-338C15.3 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 = 'RP11-338C15.3' 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
Q40.141
Q40
Are there any specific alleles within the gene SLC6A13 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood and Liver samples tested, there are no alleles within the gene SLC6A13 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 = 'SLC6A13' 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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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.900
Q40
Are there any specific alleles within the gene SOCS2 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 SOCS2 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 = 'SOCS2' 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
Q40.1839
Q40
Are there any specific alleles within the gene GLI2 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene GLI2 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 = 'GLI2' 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
Q40.555
Q40
Are there any specific alleles within the gene AC138969.4 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Skeletal Muscle samples tested, there are no alleles within the gene AC138969.4 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 = 'AC138969.4' 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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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.323
Q40
Are there any specific alleles within the gene ACTL7B associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene ACTL7B 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 = 'ACTL7B' 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
Q40.1854
Q40
Are there any specific alleles within the gene SLC30A5 associated with increased susceptibility to developing Alzheimer's Disease, 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 SLC30A5 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 = 'SLC30A5' 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
Q40.1235
Q40
Are there any specific alleles within the gene GLE1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Whole Blood, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene GLE1 that are sig...
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 = 'GLE1' 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
Q40.1726
Q40
Are there any specific alleles within the gene AC000068.9 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Skeletal Muscle samples tested, there are no alleles within the gene AC000068.9 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 = 'AC000068.9' 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
Q40.564
Q40
Are there any specific alleles within the gene RP11-257P3.3 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 RP11-257P3.3 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 = 'RP11-257P3.3' 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
Q40.142
Q40
Are there any specific alleles within the gene SETD2 associated with increased susceptibility to developing Lewy Body 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 SETD2 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 = 'SETD2' 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
Q40.1736
Q40
Are there any specific alleles within the gene TPRX1 associated with increased susceptibility to developing Parkinson'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 TPRX1 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 = 'TPRX1' 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
Q40.537
Q40
Are there any specific alleles within the gene RBBP5 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, Multi Ancestry Whole Brain and Nucleus Accumbens Basal samples tested, there are no alleles within the gene RBBP5 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 = 'RBBP5' 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
Q40.227
Q40
Are there any specific alleles within the gene RP11-578F21.9 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 RP11-578F21.9 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 = 'RP11-578F21.9' 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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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.730
Q40
Are there any specific alleles within the gene RP11-445H22.3 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex, Whole Blood and Whole Brain samples tested, there are no alleles within the gene RP11-445H22.3 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 = 'RP11-445H22.3' 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
Q40.793
Q40
Are there any specific alleles within the gene TPM3P9 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Substantia nigra, Hypothalamus, Liver, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala, Cerebellum a...
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 = 'TPM3P9' 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
Q40.1718
Q40
Are there any specific alleles within the gene RP11-54K16.2 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Tibial Nerve samples tested, there are no alleles within the gene RP11-54K16.2 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 = 'RP11-54K16.2' 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
Q40.994
Q40
Are there any specific alleles within the gene ZFR 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 ZFR 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 = 'ZFR' 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
Q40.415
Q40
Are there any specific alleles within the gene SPATA33 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, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain and Anterior Cingulate Cortex BA24 samples tested, there are no alleles within the gene SPATA33 that are significantly ...
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 = 'SPATA33' 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
Q40.329
Q40
Are there any specific alleles within the gene CTC-304I17.5 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere and Cerebellum samples tested, there are no alleles within the gene CTC-304I17.5 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 = 'CTC-304I17.5' 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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SMR Significance, Effect
Q40.1098
Q40
Are there any specific alleles within the gene SPINT2 associated with increased susceptibility to developing Progressive supranuclear palsy, 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 SPINT2 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 = 'SPINT2' 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
Q40.303
Q40
Are there any specific alleles within the gene CAPZA1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Cortex, Cerebellar Hemisphere, Tibial Nerve, Multi Ancestry Whole Brain, Whole Blood and Nucleus Accumbens Basal samples tested, there are no alleles within the gene CAPZA1 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 = 'CAPZA1' 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
Q40.1259
Q40
Are there any specific alleles within the gene COX19 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene COX19 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 = 'COX19' 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
Q40.1996
Q40
Are there any specific alleles within the gene RP11-325P15.1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Blood and Cerebellum samples tested, there are no alleles within the gene RP11-325P15.1 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 = 'RP11-325P15.1' 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
Q40.26
Q40
Are there any specific alleles within the gene GATS associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene GATS that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs1636988 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.26e-11; b: 1.0598e-01 • rs1727133 • Skeletal Muscle: Adjusted SMR multi-SNP P-value: 6.13e-07; b: 3.451...
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 = 'GATS' 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_585988', 'Gene': 'GATS', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs1636988', 'A1': 'G', 'A2': 'A', 'Freq': 0.262781, 'p_SMR_multi': 1.261396e-11, 'Disease': 'AD', 'b_SMR': 0.105982, 'p_HEIDI': 7.181786e-05}, {'UUID': 'NDD_SMR_genes_all_update_text_1340318', 'Gene': 'GATS', 'Omi...
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SMR Significance, Effect
Q40.1860
Q40
Are there any specific alleles within the gene BCL6B associated with increased susceptibility to developing Lewy Body 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 BCL6B 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 = 'BCL6B' 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