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Q40.873
Q40
Are there any specific alleles within the gene FBN3 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 Skeletal Muscle samples tested, there are no alleles within the gene FBN3 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 = 'FBN3' 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
Q40.47
Q40
Are there any specific alleles within the gene BPIFC associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Blood and Tibial Nerve samples tested, there are no alleles within the gene BPIFC 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 = 'BPIFC' 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
Q40.1388
Q40
Are there any specific alleles within the gene TMEM134 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 TMEM134 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 = 'TMEM134' 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
Q40.1709
Q40
Are there any specific alleles within the gene PLPP4 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cerebellum samples tested, there are no alleles within the gene PLPP4 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 = 'PLPP4' 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
Q40.1000
Q40
Are there any specific alleles within the gene DGKE associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Multi Ancestry Whole Brain, Whole Blood and Whole Brain samples tested, there are no alleles within the gene DGKE 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 = 'DGKE' 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
Q40.883
Q40
Are there any specific alleles within the gene SLC25A33 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene SLC25A33 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 = 'SLC25A33' 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
Q40.780
Q40
Are there any specific alleles within the gene KCNK3 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 Multi Ancestry Whole Brain samples tested, there are no alleles within the gene KCNK3 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 = 'KCNK3' 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
Q40.1229
Q40
Are there any specific alleles within the gene RP11-707O23.5 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
Yes, there are 3 alleles within the gene RP11-707O23.5 that are significantly associated with an increased susceptibility to developing Progressive supranuclear palsy: • rs12373139 • Skeletal Muscle: Adjusted SMR multi-SNP P-value: 5.87e-34; b: 1.4198e+00 • Tibial Nerve: Adjusted SMR multi-SNP P-value: 1.03e-28...
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 = '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_1375926', 'Gene': 'RP11-707O23.5', 'Omic_tissue': 'Skeletal Muscle', 'topSNP': 'rs12373139', 'A1': 'A', 'A2': 'G', 'Freq': 0.235174, 'p_SMR_multi': 5.871314e-34, 'Disease': 'PSP', 'b_SMR': 1.41982, 'p_HEIDI': 1.452029e-26}, {'UUID': 'NDD_SMR_genes_all_update_text_1684932', 'Gene...
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SMR Significance, Effect
Q40.2000
Q40
Are there any specific alleles within the gene C15orf57 associated with increased susceptibility to developing Parkinson'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 = 'C15orf57' 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
Q40.5
Q40
Are there any specific alleles within the gene RP3-510D11.1 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 RP3-510D11.1 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 = 'RP3-510D11.1' 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
Q40.1012
Q40
Are there any specific alleles within the gene RP11-214O1.2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex, Tibial Nerve, Skeletal Muscle and Whole Blood samples tested, there are no alleles within the gene RP11-214O1.2 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 = 'RP11-214O1.2' 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
Q40.1724
Q40
Are there any specific alleles within the gene MRPL48 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, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain and Liver samples tested, there are no alleles within the gene MRPL48 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 = 'MRPL48' 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
Q40.266
Q40
Are there any specific alleles within the gene AXL 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, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene AXL 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 = 'AXL' 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
Q40.1570
Q40
Are there any specific alleles within the gene MED26 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 MED26 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 = 'MED26' 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
Q40.1832
Q40
Are there any specific alleles within the gene AMPD3 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Basal Ganglia, Spinalcord, Hippocampus, Whole Brain, Whole Blood, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Putamen Basal Ganglia, Amygdala and Nucleus Accumbens Basal samples tested, there are no alleles within the gene AMPD3 that are significantly assoc...
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 = 'AMPD3' 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
Q40.449
Q40
Are there any specific alleles within the gene GNRHR2P1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex samples tested, there are no alleles within the gene GNRHR2P1 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 = 'GNRHR2P1' 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
Q40.1011
Q40
Are there any specific alleles within the gene RP1-66C13.3 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 RP1-66C13.3 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 = 'RP1-66C13.3' 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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SMR Significance, Effect
Q40.1086
Q40
Are there any specific alleles within the gene CTD-2514C3.1 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 CTD-2514C3.1 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 = 'CTD-2514C3.1' 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
Q40.844
Q40
Are there any specific alleles within the gene ASB13 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, Prefrontal Cortex, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene ASB13 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 = 'ASB13' 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
Q40.1792
Q40
Are there any specific alleles within the gene GPR179 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Brain and Cortex samples tested, there are no alleles within the gene GPR179 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 = 'GPR179' 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
Q40.308
Q40
Are there any specific alleles within the gene IL1F10 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 IL1F10 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 = 'IL1F10' 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
Q40.1380
Q40
Are there any specific alleles within the gene HIST1H2BN associated with increased susceptibility to developing Parkinson's Disease, 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 HIST1H2BN 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 = 'HIST1H2BN' 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
Q40.1558
Q40
Are there any specific alleles within the gene MCM10 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Tibial Nerve and Skeletal Muscle samples tested, there are no alleles within the gene MCM10 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 = 'MCM10' 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
Q40.317
Q40
Are there any specific alleles within the gene AP001055.1 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 AP001055.1 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 = 'AP001055.1' 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
Q40.152
Q40
Are there any specific alleles within the gene RP11-521O16.1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 3 alleles within the gene RP11-521O16.1 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs77571924 • Whole Blood: Adjusted SMR multi-SNP P-value: 4.48e-17; b: 3.2588e-02 • rs2404175 • Whole Blood: Adjusted SMR multi-SNP P-value: 3.72e-15; 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 = 'RP11-521O16.1' 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_631109', 'Gene': 'RP11-521O16.1', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs77571924', 'A1': 'A', 'A2': 'T', 'Freq': 0.137014, 'p_SMR_multi': 4.4846810000000005e-17, 'Disease': 'AD', 'b_SMR': 0.0325877, 'p_HEIDI': 1.460436e-09}, {'UUID': 'NDD_SMR_genes_all_update_text_631110', ...
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SMR Significance, Effect
Q40.1158
Q40
Are there any specific alleles within the gene FAM63B associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene FAM63B that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs395601 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.93e-06; b: 8.8978e-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 = 'FAM63B' 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_646471', 'Gene': 'FAM63B', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs395601', 'A1': 'C', 'A2': 'G', 'Freq': 0.421268, 'p_SMR_multi': 2.925908e-06, 'Disease': 'AD', 'b_SMR': 0.0889776, 'p_HEIDI': 0.0005645899}]
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SMR Significance, Effect
Q40.1223
Q40
Are there any specific alleles within the gene RNF139 associated with increased susceptibility to developing Lewy Body Dementia, 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 RNF139 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 = 'RNF139' 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
Q40.580
Q40
Are there any specific alleles within the gene FOXR1 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 FOXR1 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 = 'FOXR1' 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
Q40.51
Q40
Are there any specific alleles within the gene DDI2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Cerebellar Hemisphere, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene DDI2 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 = 'DDI2' 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
Q40.1553
Q40
Are there any specific alleles within the gene TM4SF4 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 TM4SF4 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 = 'TM4SF4' 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
Q40.733
Q40
Are there any specific alleles within the gene ZNF576 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 ZNF576 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 = 'ZNF576' 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
Q40.840
Q40
Are there any specific alleles within the gene STK11 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 STK11 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 = 'STK11' 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
Q40.1392
Q40
Are there any specific alleles within the gene ARHGAP27 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene ARHGAP27 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs35489312 • Whole Blood: Adjusted SMR multi-SNP P-value: 5.52e-07; b: 3.8537e-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 = 'ARHGAP27' 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_591157', 'Gene': 'ARHGAP27', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs35489312', 'A1': 'C', 'A2': 'T', 'Freq': 0.190184, 'p_SMR_multi': 5.523958e-07, 'Disease': 'AD', 'b_SMR': 0.0385365, 'p_HEIDI': 0.01412357}, {'UUID': 'NDD_SMR_genes_all_update_text_591156', 'Gene': 'ARHGAP27...
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SMR Significance, Effect
Q40.1125
Q40
Are there any specific alleles within the gene CTD-2561B21.3 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-2561B21.3 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 = 'CTD-2561B21.3' 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
Q40.1176
Q40
Are there any specific alleles within the gene C6orf3 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Frontal Cortex, Cerebellar Hemisphere, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Hypothalamus, Anterior Cingulate Cortex BA24, Whole Blood, Putamen Basal Ganglia, Whole Brain, Cerebellum and Nucleus Accumbens Basal samples tested, there are n...
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 = 'C6orf3' 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
Q40.476
Q40
Are there any specific alleles within the gene OR2T4 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex and Prefrontal Cortex samples tested, there are no alleles within the gene OR2T4 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 = 'OR2T4' 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
Q40.980
Q40
Are there any specific alleles within the gene SMPD1 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellum and Whole Blood samples tested, there are no alleles within the gene SMPD1 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 = 'SMPD1' 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
Q40.660
Q40
Are there any specific alleles within the gene SNCA associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene SNCA that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs6817026 • Whole Brain: Adjusted SMR multi-SNP P-value: 1.92e-10; b: 4.5665e-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 = 'SNCA' 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_432416', 'Gene': 'SNCA', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs6817026', 'A1': 'C', 'A2': 'T', 'Freq': 0.515337, 'p_SMR_multi': 1.918689e-10, 'Disease': 'PD', 'b_SMR': 0.0456646, 'p_HEIDI': 3.752528e-09}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.405
Q40
Are there any specific alleles within the gene STYX associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene STYX that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs77690283 • Skeletal Muscle: Adjusted SMR multi-SNP P-value: 8.21e-08; b: 1.5066e-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 = 'STYX' 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_1342185', 'Gene': 'STYX', 'Omic_tissue': 'Skeletal Muscle', 'topSNP': 'rs77690283', 'A1': 'G', 'A2': 'C', 'Freq': 0.097137, 'p_SMR_multi': 8.214654e-08, 'Disease': 'AD', 'b_SMR': 0.150658, 'p_HEIDI': 0.005807537}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.517
Q40
Are there any specific alleles within the gene FAM215B associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene FAM215B that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs7218567 • Whole Brain: Adjusted SMR multi-SNP P-value: 2.53e-08; b: 1.3970e-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 = 'FAM215B' 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_1640231', 'Gene': 'FAM215B', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs7218567', 'A1': 'C', 'A2': 'A', 'Freq': 0.712679, 'p_SMR_multi': 2.52907e-08, 'Disease': 'PD', 'b_SMR': 0.139698, 'p_HEIDI': 0.00431549}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.324
Q40
Are there any specific alleles within the gene PIGB associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Frontal Cortex, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene PIGB 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 = 'PIGB' 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
Q40.20
Q40
Are there any specific alleles within the gene NDUFB9 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Prefrontal Cortex and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene NDUFB9 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 = 'NDUFB9' 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
Q40.691
Q40
Are there any specific alleles within the gene AP001619.2 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain and Cerebellum samples tested, there are no alleles within the gene AP001619.2 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 = 'AP001619.2' 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
Q40.36
Q40
Are there any specific alleles within the gene KDM8 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Cortex, Skeletal Muscle, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene KDM8 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 = 'KDM8' 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
Q40.910
Q40
Are there any specific alleles within the gene PRCD associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Cortex, Tibial Nerve, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene PRCD 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 = 'PRCD' 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
Q40.834
Q40
Are there any specific alleles within the gene ATP13A4-AS1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cortex and Nucleus Accumbens Basal samples tested, there are no alleles within the gene ATP13A4-AS1 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 = 'ATP13A4-AS1' 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
Q40.1798
Q40
Are there any specific alleles within the gene SMIM19 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Basal Ganglia, Spinalcord, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Substantia nigra, Hypothalamus, Liver, Anterior Cingulate Cortex BA24, Putamen Basal Gangl...
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 = 'SMIM19' 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
Q40.413
Q40
Are there any specific alleles within the gene VPS4B 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 VPS4B 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 = 'VPS4B' 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
Q40.928
Q40
Are there any specific alleles within the gene LMTK2 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 LMTK2 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 = 'LMTK2' 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
Q40.543
Q40
Are there any specific alleles within the gene TAX1BP3 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Cortex, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Whole Blood and Whole Brain samples tested, there are no alleles within the gene TAX1BP3 that are significantly associated with an increased susceptibility to developing Alzheimer's ...
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 = 'TAX1BP3' 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
Q40.765
Q40
Are there any specific alleles within the gene TAP2 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene TAP2 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs4148876 • Whole Blood: Adjusted SMR multi-SNP P-value: 9.94e-08; b: 4.4688e-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 = 'TAP2' 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_1494776', 'Gene': 'TAP2', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs4148876', 'A1': 'A', 'A2': 'G', 'Freq': 0.0756646, 'p_SMR_multi': 9.936974e-08, 'Disease': 'AD', 'b_SMR': 0.0446882, 'p_HEIDI': 0.0001713229}]
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SMR Significance, Effect
Q40.1905
Q40
Are there any specific alleles within the gene RP11-159H22.2 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 RP11-159H22.2 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 = 'RP11-159H22.2' 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
Q40.1071
Q40
Are there any specific alleles within the gene SIAH2 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 SIAH2 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 = 'SIAH2' 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
Q40.1209
Q40
Are there any specific alleles within the gene CCDC9 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Tibial Nerve, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene CCDC9 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 = 'CCDC9' 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
Q40.248
Q40
Are there any specific alleles within the gene RP11-123M21.1 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 RP11-123M21.1 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 = 'RP11-123M21.1' 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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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1431
Q40
Are there any specific alleles within the gene AC005726.1 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 AC005726.1 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 = 'AC005726.1' 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
Q40.1137
Q40
Are there any specific alleles within the gene SSC4D 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 SSC4D 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 = 'SSC4D' 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
Q40.791
Q40
Are there any specific alleles within the gene RP11-491F9.8 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere and Cerebellum samples tested, there are no alleles within the gene RP11-491F9.8 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 = 'RP11-491F9.8' 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
Q40.1744
Q40
Are there any specific alleles within the gene UBAC2-AS1 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 UBAC2-AS1 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 = 'UBAC2-AS1' 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
Q40.495
Q40
Are there any specific alleles within the gene RP11-101O21.1 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 RP11-101O21.1 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 = 'RP11-101O21.1' 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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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.157
Q40
Are there any specific alleles within the gene RANBP1 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 RANBP1 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 = 'RANBP1' 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
Q40.970
Q40
Are there any specific alleles within the gene MCHR2 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex and Nucleus Accumbens Basal samples tested, there are no alleles within the gene MCHR2 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 = 'MCHR2' 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
Q40.860
Q40
Are there any specific alleles within the gene AC005606.14 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 AC005606.14 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 = 'AC005606.14' 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
Q40.1325
Q40
Are there any specific alleles within the gene ITGA11 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 ITGA11 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 = 'ITGA11' 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
Q40.632
Q40
Are there any specific alleles within the gene DOC2A associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 9 alleles within the gene DOC2A that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs12921753 • Whole Blood: Adjusted SMR multi-SNP P-value: 5.58e-12; b: 4.2445e-02 • rs12596543 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.06e-08; b: 9.7466...
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 = 'DOC2A' 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_577418', 'Gene': 'DOC2A', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs12921753', 'A1': 'T', 'A2': 'C', 'Freq': 0.380368, 'p_SMR_multi': 5.575261e-12, 'Disease': 'AD', 'b_SMR': 0.0424449, 'p_HEIDI': 0.3441697}, {'UUID': 'NDD_SMR_genes_all_update_text_577419', 'Gene': 'DOC2A', 'Omi...
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SMR Significance, Effect
Q40.692
Q40
Are there any specific alleles within the gene LGALS17A associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Skeletal Muscle and Whole Blood samples tested, there are no alleles within the gene LGALS17A 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 = 'LGALS17A' 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
Q40.1562
Q40
Are there any specific alleles within the gene FAM179A associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Frontal Cortex, Prefrontal Cortex, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Hypothalamus, Liver, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala and Nucleus Accumbens Basal samples tested, there are ...
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 = 'FAM179A' 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
Q40.575
Q40
Are there any specific alleles within the gene TRAV12-2 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 TRAV12-2 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 = 'TRAV12-2' 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
Q40.1909
Q40
Are there any specific alleles within the gene RP11-249C24.10 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 RP11-249C24.10 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 = 'RP11-249C24.10' 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
Q40.18
Q40
Are there any specific alleles within the gene SLC29A4 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 Liver samples tested, there are no alleles within the gene SLC29A4 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 = 'SLC29A4' 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
Q40.130
Q40
Are there any specific alleles within the gene C19orf68 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 C19orf68 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 = 'C19orf68' 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
Q40.1361
Q40
Are there any specific alleles within the gene HSPA8P18 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex and Tibial Nerve samples tested, there are no alleles within the gene HSPA8P18 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 = 'HSPA8P18' 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
Q40.1291
Q40
Are there any specific alleles within the gene AC009133.14 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 AC009133.14 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 = 'AC009133.14' 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
Q40.1969
Q40
Are there any specific alleles within the gene CTC-542B22.1 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 CTC-542B22.1 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 = 'CTC-542B22.1' 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
Q40.935
Q40
Are there any specific alleles within the gene TRAF7 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 TRAF7 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 = 'TRAF7' 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
Q40.989
Q40
Are there any specific alleles within the gene RP11-334J6.6 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 RP11-334J6.6 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 = 'RP11-334J6.6' 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
Q40.1965
Q40
Are there any specific alleles within the gene RP11-950C14.7 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, 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 RP11-950C14.7 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 = 'RP11-950C14.7' 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
Q40.193
Q40
Are there any specific alleles within the gene AC013264.2 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 AC013264.2 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 = 'AC013264.2' 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
Q40.1149
Q40
Are there any specific alleles within the gene DSG3 associated with increased susceptibility to developing Parkinson's Disease, 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 DSG3 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 = 'DSG3' 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
Q40.1001
Q40
Are there any specific alleles within the gene NAALAD2 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Cortex, Prefrontal Cortex, Tibial Nerve, Hippocampus, Multi Ancestry Whole Brain, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene NAALAD2 that are significantly associated with an increased susceptibility to developing Amy...
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 = 'NAALAD2' 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
Q40.1956
Q40
Are there any specific alleles within the gene RP11-21B21.4 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, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Cerebellum and Nucleus Accumbens Basal samples tested, there are no alleles within the gene RP11-21B21.4 that are significantly associated with an increased susceptibility to developing Parkin...
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 = 'RP11-21B21.4' 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
Q40.1657
Q40
Are there any specific alleles within the gene MLF1 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, Skeletal Muscle, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene MLF1 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 = 'MLF1' 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
Q40.613
Q40
Are there any specific alleles within the gene MYBPC3 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene MYBPC3 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs11039200 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.15e-07; b: 6.4532e-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 = 'MYBPC3' 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_1498212', 'Gene': 'MYBPC3', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs11039200', 'A1': 'C', 'A2': 'A', 'Freq': 0.315951, 'p_SMR_multi': 1.146533e-07, 'Disease': 'AD', 'b_SMR': 0.0645316, 'p_HEIDI': 0.008616443}]
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SMR Significance, Effect
Q40.183
Q40
Are there any specific alleles within the gene LPCAT1 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 LPCAT1 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 = 'LPCAT1' 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
Q40.305
Q40
Are there any specific alleles within the gene CYP2F1 associated with increased susceptibility to developing Parkinson's Disease, 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 CYP2F1 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 = 'CYP2F1' 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
Q40.502
Q40
Are there any specific alleles within the gene SPI1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene SPI1 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs11570034 • Whole Blood: Adjusted SMR multi-SNP P-value: 3.74e-07; b: 2.0233e-02 • rs12801188 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.27e-06; b: 1.7636e...
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 = 'SPI1' 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_1498213', 'Gene': 'SPI1', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs11570034', 'A1': 'G', 'A2': 'A', 'Freq': 0.0296524, 'p_SMR_multi': 3.736983e-07, 'Disease': 'AD', 'b_SMR': 0.0202333, 'p_HEIDI': 0.437956}, {'UUID': 'NDD_SMR_genes_all_update_text_608486', 'Gene': 'SPI1', 'Omic...
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SMR Significance, Effect
Q40.1696
Q40
Are there any specific alleles within the gene SRD5A3 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, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Liver and Putamen Basal Ganglia samples tested, there are no alleles within the gene SRD5A3 that are significantly assoc...
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 = 'SRD5A3' 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
Q40.1721
Q40
Are there any specific alleles within the gene C3orf39 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 C3orf39 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 = 'C3orf39' 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
Q40.1662
Q40
Are there any specific alleles within the gene NAV1 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 NAV1 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 = 'NAV1' 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
Q40.1639
Q40
Are there any specific alleles within the gene LINC01140 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene LINC01140 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 = 'LINC01140' 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
Q40.523
Q40
Are there any specific alleles within the gene AJUBA 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 AJUBA 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 = 'AJUBA' 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
Q40.1985
Q40
Are there any specific alleles within the gene RP11-95D17.1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Liver, Whole Blood and Cerebellum samples tested, there are no alleles within the gene RP11-95D17.1 that are significantly associated with an increased susceptibility to developing Amyotrophic Lateral S...
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 = 'RP11-95D17.1' 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
Q40.1078
Q40
Are there any specific alleles within the gene POGK associated with increased susceptibility to developing Progressive supranuclear palsy, 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 POGK 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 = 'POGK' 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
Q40.482
Q40
Are there any specific alleles within the gene SCARNA24 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 SCARNA24 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 = 'SCARNA24' 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
Q40.160
Q40
Are there any specific alleles within the gene ARID4A 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 ARID4A 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 = 'ARID4A' 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
Q40.1253
Q40
Are there any specific alleles within the gene C20orf144 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene C20orf144 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 = 'C20orf144' 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
Q40.1205
Q40
Are there any specific alleles within the gene OS9 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 OS9 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 = 'OS9' 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
Q40.17
Q40
Are there any specific alleles within the gene CSTF1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene CSTF1 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs6024857 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.11e-10; b: 3.3751e-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 = 'CSTF1' 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_1504669', 'Gene': 'CSTF1', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs6024857', 'A1': 'C', 'A2': 'T', 'Freq': 0.122699, 'p_SMR_multi': 2.112683e-10, 'Disease': 'AD', 'b_SMR': 0.337511, 'p_HEIDI': 1.254673e-05}]
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SMR Significance, Effect
Q40.1550
Q40
Are there any specific alleles within the gene PNKD associated with increased susceptibility to developing Progressive supranuclear palsy, 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 PNKD 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 = 'PNKD' 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
Q40.1081
Q40
Are there any specific alleles within the gene SPPL2A 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, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain and Liver samples tested, there are no alleles within the gene SPPL2A that are significantly associated with an increased susceptibility to developing Am...
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 = 'SPPL2A' 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