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Q40.978
Q40
Are there any specific alleles within the gene CEP41 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Blood, Cortex, Tibial Nerve, Multi Ancestry Whole Brain and Whole Brain samples tested, there are no alleles within the gene CEP41 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 = 'CEP41' 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
Q40.611
Q40
Are there any specific alleles within the gene PKD1L1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Cortex, Frontal Cortex, Cerebellar Hemisphere, 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 PKD1L1 that are significantly associated with an increased sus...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'PKD1L1' 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
Q40.1919
Q40
Are there any specific alleles within the gene UBA7 associated with increased susceptibility to developing Frontotemporal Dementia, 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 UBA7 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 = 'UBA7' 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
Q40.92
Q40
Are there any specific alleles within the gene NCR1 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 NCR1 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 = 'NCR1' 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
Q40.855
Q40
Are there any specific alleles within the gene DDT associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Spinalcord, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Hypothalamus, Liver, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia and Nucleus Accum...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'DDT' 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
Q40.1521
Q40
Are there any specific alleles within the gene MIR4635 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 MIR4635 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 = 'MIR4635' 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
Q40.1918
Q40
Are there any specific alleles within the gene CRHR1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 3 alleles within the gene CRHR1 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs17689882 • Whole Blood: Adjusted SMR multi-SNP P-value: 3.89e-07; b: 5.7883e-02 • rs79923708 • Prefrontal Cortex: Adjusted SMR multi-SNP P-value: 5.84e-07; 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 = 'CRHR1' 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_591172', 'Gene': 'CRHR1', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs17689882', 'A1': 'A', 'A2': 'G', 'Freq': 0.234151, 'p_SMR_multi': 3.894906e-07, 'Disease': 'AD', 'b_SMR': 0.0578831, 'p_HEIDI': 0.008599073}, {'UUID': 'NDD_SMR_genes_all_update_text_1203006', 'Gene': 'CRHR1', '...
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SMR Significance, Effect
Q40.760
Q40
Are there any specific alleles within the gene CLIC6 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Substantia nigra and Putamen Basal Ganglia samples tested, there are no alleles within the gene CLIC6 that are significantly associated with...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CLIC6' 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
Q40.504
Q40
Are there any specific alleles within the gene CTC-559E9.10 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere and Cerebellum samples tested, there are no alleles within the gene CTC-559E9.10 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 = 'CTC-559E9.10' 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
Q40.1287
Q40
Are there any specific alleles within the gene CPNE6 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 CPNE6 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 = 'CPNE6' 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
Q40.1340
Q40
Are there any specific alleles within the gene RP11-448P19.1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene RP11-448P19.1 that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs10750540 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.43e-07; b: 8.3291e-02
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-448P19.1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_961094', 'Gene': 'RP11-448P19.1', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs10750540', 'A1': 'G', 'A2': 'C', 'Freq': 0.395706, 'p_SMR_multi': 1.434394e-07, 'Disease': 'PD', 'b_SMR': 0.0832914, 'p_HEIDI': 0.004974471}, {'UUID': 'NDD_SMR_genes_all_update_text_961091', 'Gene': 'RP...
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SMR Significance, Effect
Q40.12
Q40
Are there any specific alleles within the gene SRFBP1 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 SRFBP1 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 = 'SRFBP1' 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
Q40.402
Q40
Are there any specific alleles within the gene RP11-473M20.14 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Frontal Cortex, Cerebellar Hemisphere, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Hypothalamus, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala, Cerebellum and Nucleus Accumbens Basal samples tested, t...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-473M20.14' 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
Q40.288
Q40
Are there any specific alleles within the gene CCDC85A associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellum, Basal Ganglia, Whole Brain, Whole Blood, Cortex, Cerebellar Hemisphere, Caudate Basal Ganglia and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene CCDC85A that are significantly associated with an increased susceptibility to developing Progressive supranuclear...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'CCDC85A' 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
Q40.1075
Q40
Are there any specific alleles within the gene AC016629.3 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Frontal Cortex, Cerebellar Hemisphere, Cortex, Tibial Nerve, Whole Brain and Cerebellum samples tested, there are no alleles within the gene AC016629.3 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 = 'AC016629.3' 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
Q40.1201
Q40
Are there any specific alleles within the gene CXCR4 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Skeletal Muscle and Whole Blood samples tested, there are no alleles within the gene CXCR4 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 = 'CXCR4' 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
Q40.1746
Q40
Are there any specific alleles within the gene CLU associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 5 alleles within the gene CLU that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs7982 • Whole Brain: Adjusted SMR multi-SNP P-value: 2.50e-10; b: 2.7261e-01 • rs34109053 • Whole Brain: Adjusted SMR multi-SNP P-value: 6.57e-09; b: 9.7224e-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 = 'CLU' 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_78262', 'Gene': 'CLU', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs7982', 'A1': 'A', 'A2': 'G', 'Freq': 0.387526, 'p_SMR_multi': 2.501744e-10, 'Disease': 'AD', 'b_SMR': 0.272613, 'p_HEIDI': 6.84878e-05}, {'UUID': 'NDD_SMR_genes_all_update_text_78266', 'Gene': 'CLU', 'Omic_tissue'...
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SMR Significance, Effect
Q40.697
Q40
Are there any specific alleles within the gene EFHA1 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 EFHA1 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 = 'EFHA1' 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
Q40.1632
Q40
Are there any specific alleles within the gene RP11-259G18.2 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene RP11-259G18.2 that are significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs578109777 • Whole Brain: Adjusted SMR multi-SNP P-value: 5.45e-09; b: 3.9113e-01 • rs199498 • Prefrontal Cortex: Adjusted SMR multi-SNP P-value: 4.70e-...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-259G18.2' 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_491154', 'Gene': 'RP11-259G18.2', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs578109777', 'A1': 'C', 'A2': 'T', 'Freq': 0.237219, 'p_SMR_multi': 5.445399e-09, 'Disease': 'PD', 'b_SMR': 0.39113, 'p_HEIDI': -9999.0}, {'UUID': 'NDD_SMR_genes_all_update_text_1242278', 'Gene': 'RP11-2...
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SMR Significance, Effect
Q40.1877
Q40
Are there any specific alleles within the gene THAP4 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, Prefrontal Cortex, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene THAP4 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 = 'THAP4' 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
Q40.696
Q40
Are there any specific alleles within the gene MEX3A 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 MEX3A 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 = 'MEX3A' AND Disease = 'PSP' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
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Q40.858
Q40
Are there any specific alleles within the gene RP11-45P15.2 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex samples tested, there are no alleles within the gene RP11-45P15.2 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 = 'RP11-45P15.2' 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
Q40.162
Q40
Are there any specific alleles within the gene RNASEH2C associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Cortex, Frontal Cortex, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Amygdala, Whole Brain, Cerebellum and Nucleus Accumbens Basal samples tested, there are no alleles within the gene RNASEH2C that are significantly associated with an increased...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RNASEH2C' 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
Q40.902
Q40
Are there any specific alleles within the gene DNMT3B associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Cerebellar Hemisphere, Tibial Nerve and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene DNMT3B 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 = 'DNMT3B' 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
Q40.1576
Q40
Are there any specific alleles within the gene IGKV1D-16 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 IGKV1D-16 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 = 'IGKV1D-16' 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
Q40.260
Q40
Are there any specific alleles within the gene MINOS1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Prefrontal Cortex, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene MINOS1 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 = 'MINOS1' 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
Q40.339
Q40
Are there any specific alleles within the gene AC024592.12 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 AC024592.12 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 = 'AC024592.12' 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
Q40.1881
Q40
Are there any specific alleles within the gene RP11-690J15.1 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Brain samples tested, there are no alleles within the gene RP11-690J15.1 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 = 'RP11-690J15.1' 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
Q40.1048
Q40
Are there any specific alleles within the gene BANF2 associated with increased susceptibility to developing Parkinson'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 BANF2 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 = 'BANF2' 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
Q40.521
Q40
Are there any specific alleles within the gene RP13-122B23.8 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 RP13-122B23.8 that are significantly associated with an increased susceptibility to developing Frontotemporal Dementia.
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP13-122B23.8' 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
Q40.1363
Q40
Are there any specific alleles within the gene NAALADL1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene NAALADL1 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 = 'NAALADL1' 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
Q40.1024
Q40
Are there any specific alleles within the gene AC010642.1 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 AC010642.1 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 = 'AC010642.1' 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
Q40.775
Q40
Are there any specific alleles within the gene ARHGDIG 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, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene ARHGDIG 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 = 'ARHGDIG' 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
Q40.1748
Q40
Are there any specific alleles within the gene RP11-385F7.1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene RP11-385F7.1 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs4715019 • Whole Brain: Adjusted SMR multi-SNP P-value: 2.22e-08; b: 9.5186e-02 • rs1931837 • Whole Blood: Adjusted SMR multi-SNP P-value: 8.36e-08; b: 1...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-385F7.1' 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_67372', 'Gene': 'RP11-385F7.1', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs4715019', 'A1': 'A', 'A2': 'T', 'Freq': 0.251534, 'p_SMR_multi': 2.218978e-08, 'Disease': 'AD', 'b_SMR': 0.0951858, 'p_HEIDI': 0.05490125}, {'UUID': 'NDD_SMR_genes_all_update_text_622987', 'Gene': 'RP11-3...
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SMR Significance, Effect
Q40.768
Q40
Are there any specific alleles within the gene C22orf9 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 C22orf9 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 = 'C22orf9' 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
Q40.1256
Q40
Are there any specific alleles within the gene HTRA4 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 HTRA4 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 = 'HTRA4' 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
Q40.1213
Q40
Are there any specific alleles within the gene DBP 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 DBP 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 = 'DBP' 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
Q40.1469
Q40
Are there any specific alleles within the gene RCAN2 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 RCAN2 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 = 'RCAN2' 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
Q40.1984
Q40
Are there any specific alleles within the gene RP11-415J8.3 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Multi Ancestry Whole Brain samples tested, there are no alleles within the gene RP11-415J8.3 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 = 'RP11-415J8.3' 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
Q40.527
Q40
Are there any specific alleles within the gene TCN1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene TCN1 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs12419784 • Whole Blood: Adjusted SMR multi-SNP P-value: 6.99e-13; b: 1.6021e-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 = 'TCN1' 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_1498258', 'Gene': 'TCN1', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs12419784', 'A1': 'A', 'A2': 'G', 'Freq': 0.264826, 'p_SMR_multi': 6.992786e-13, 'Disease': 'AD', 'b_SMR': 0.160213, 'p_HEIDI': 4.993905e-07}]
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SMR Significance, Effect
Q40.23
Q40
Are there any specific alleles within the gene CDADC1 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellum, Cortex, Cerebellar Hemisphere, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Whole Blood and Whole Brain samples tested, there are no alleles within the gene CDADC1 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 = 'CDADC1' 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
Q40.361
Q40
Are there any specific alleles within the gene HAR1B associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Cortex, Caudate Basal Ganglia, Hypothalamus, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala, Cerebellum and Nucleus Accumbens Basal samples tested, there are no alleles within the gene HAR1B that are si...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'HAR1B' 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
Q40.1288
Q40
Are there any specific alleles within the gene EMILIN3 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Hippocampus, Whole Brain, Whole Blood, Cortex, Caudate Basal Ganglia, Multi Ancestry Whole Brain, Hypothalamus, Liver, Putamen Basal Ganglia, Amygdala and Nucleus Accumbens Basal samples tested, there are no alleles within the gene EMILIN3 that are significantly associated with an increased susceptibil...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'EMILIN3' 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
Q40.1326
Q40
Are there any specific alleles within the gene SLK 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 SLK 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 = 'SLK' 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
Q40.1683
Q40
Are there any specific alleles within the gene RP11-67M1.1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene RP11-67M1.1 that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs1551980 • Whole Brain: Adjusted SMR multi-SNP P-value: 8.24e-08; b: 1.2039e-01
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RP11-67M1.1' AND Disease = 'PD' AND p_SMR_multi < 2.95e-6 AND b_SMR > 0 ORDER BY p_SMR_multi LIMIT 100
[{'UUID': 'NDD_SMR_genes_all_update_text_432422', 'Gene': 'RP11-67M1.1', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs1551980', 'A1': 'G', 'A2': 'A', 'Freq': 0.707566, 'p_SMR_multi': 8.239773e-08, 'Disease': 'PD', 'b_SMR': 0.120394, 'p_HEIDI': 0.0001788494}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.344
Q40
Are there any specific alleles within the gene ANKRD11 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 ANKRD11 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 = 'ANKRD11' 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
Q40.437
Q40
Are there any specific alleles within the gene H1FX-AS1 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 H1FX-AS1 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 = 'H1FX-AS1' 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
Q40.479
Q40
Are there any specific alleles within the gene SPSB3 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 SPSB3 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 = 'SPSB3' 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
Q40.220
Q40
Are there any specific alleles within the gene TMEM53 associated with increased susceptibility to developing Alzheimer'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 TMEM53 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 = 'TMEM53' 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
Q40.919
Q40
Are there any specific alleles within the gene DTNA associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Cortex, Prefrontal Cortex and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene DTNA 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 = 'DTNA' 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
Q40.1237
Q40
Are there any specific alleles within the gene ARNT associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Hippocampus, Whole Brain, Whole Blood, Cortex, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene ARNT 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 = 'ARNT' 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
Q40.1597
Q40
Are there any specific alleles within the gene HNRNPCP4 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellar Hemisphere, Tibial Nerve and Cerebellum samples tested, there are no alleles within the gene HNRNPCP4 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 = 'HNRNPCP4' 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
Q40.1020
Q40
Are there any specific alleles within the gene OR2A1 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 OR2A1 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 = 'OR2A1' 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
Q40.1950
Q40
Are there any specific alleles within the gene WDPCP associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain and Whole Blood samples tested, there are no alleles within the gene WDPCP 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 = 'WDPCP' 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
Q40.96
Q40
Are there any specific alleles within the gene AC097724.3 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 AC097724.3 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 = 'AC097724.3' 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
Q40.1017
Q40
Are there any specific alleles within the gene CMTM8 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene CMTM8 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 = 'CMTM8' 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
Q40.1079
Q40
Are there any specific alleles within the gene CTC-563A5.2 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 CTC-563A5.2 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 = 'CTC-563A5.2' 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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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1101
Q40
Are there any specific alleles within the gene DNAAF4 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 DNAAF4 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 = 'DNAAF4' 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
Q40.1586
Q40
Are there any specific alleles within the gene SELL associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Basal Ganglia, Cortex, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Hippocampus, Multi Ancestry Whole Brain, Whole Blood, Putamen Basal Ganglia, Whole Brain and Nucleus Accumbens Basal samples tested, there are no alleles within the gene SELL that are significantly associated wit...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SELL' 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
Q40.1321
Q40
Are there any specific alleles within the gene MUC7 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 MUC7 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 = 'MUC7' 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
Q40.703
Q40
Are there any specific alleles within the gene RP11-277P12.9 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 RP11-277P12.9 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 = 'RP11-277P12.9' 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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SMR Significance, Effect
Q40.1794
Q40
Are there any specific alleles within the gene HAND2 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene HAND2 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 = 'HAND2' 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
Q40.1005
Q40
Are there any specific alleles within the gene CTD-2127H9.1 associated with increased susceptibility to developing Alzheimer's Disease, 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 CTD-2127H9.1 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 = 'CTD-2127H9.1' 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
Q40.156
Q40
Are there any specific alleles within the gene AC123768.1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex samples tested, there are no alleles within the gene AC123768.1 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 = 'AC123768.1' 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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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1108
Q40
Are there any specific alleles within the gene SYTL3 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 SYTL3 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 = 'SYTL3' 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
Q40.1719
Q40
Are there any specific alleles within the gene NDUFAF2 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene NDUFAF2 that is significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs2619893 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.32e-08; b: 8.0523e-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 = 'NDUFAF2' 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_1556333', 'Gene': 'NDUFAF2', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs2619893', 'A1': 'T', 'A2': 'C', 'Freq': 0.385481, 'p_SMR_multi': 1.315685e-08, 'Disease': 'PD', 'b_SMR': 0.805234, 'p_HEIDI': 0.004024545}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1998
Q40
Are there any specific alleles within the gene NUP42 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene NUP42 that are significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs2286272 • Cortex: Adjusted SMR multi-SNP P-value: 5.69e-08; b: 1.3280e-01 • rs10279691 • Cerebellum: Adjusted SMR multi-SNP P-value: 8.87e-08; b: 1.0414e-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 = 'NUP42' 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_1146422', 'Gene': 'NUP42', 'Omic_tissue': 'Cortex', 'topSNP': '7:23184748:rs2286272:T_C', 'A1': 'T', 'A2': 'C', 'Freq': 0.671779, 'p_SMR_multi': 5.686312e-08, 'Disease': 'PD', 'b_SMR': 0.132799, 'p_HEIDI': 0.07819106}, {'UUID': 'NDD_SMR_genes_all_update_text_20282', 'Gene': 'NUP...
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SMR Significance, Effect
Q40.796
Q40
Are there any specific alleles within the gene HSPE1P18 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 HSPE1P18 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 = 'HSPE1P18' 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
Q40.587
Q40
Are there any specific alleles within the gene GLG1 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Whole Brain, Cortex, Tibial Nerve and Whole Blood samples tested, there are no alleles within the gene GLG1 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 = 'GLG1' 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
Q40.710
Q40
Are there any specific alleles within the gene OR7D2 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, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle and Anterior Cingulate Cortex BA24 samples tested, there are no alleles within the gene OR7D2 that are significantly associated with an increased susceptibility to developing Progressive supranuclear pals...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'OR7D2' 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
Q40.1222
Q40
Are there any specific alleles within the gene IGHV3-74 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 IGHV3-74 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 = 'IGHV3-74' 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
Q40.1308
Q40
Are there any specific alleles within the gene FAM149A associated with increased susceptibility to developing Lewy Body Dementia, 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, Hypothalamus, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala and Nucleus...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'FAM149A' 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
Q40.1666
Q40
Are there any specific alleles within the gene ITGAX associated with increased susceptibility to developing Parkinson'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 Parkinson's Disease: • rs11574631 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.59e-07; b: 5.3384e-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 = '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_1563822', 'Gene': 'ITGAX', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs11574631', 'A1': 'C', 'A2': 'T', 'Freq': 0.315951, 'p_SMR_multi': 2.59174e-07, 'Disease': 'PD', 'b_SMR': 0.0533835, 'p_HEIDI': 0.08362627}]
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Select, Order By, Multi-Filter, Threshold
SMR Significance, Effect
Q40.1270
Q40
Are there any specific alleles within the gene HTR1D 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, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia and Nucleus Accumbens Basal samples tested, there are no alleles within the gene HTR1D that are significantly associated with an increased susceptibility to developin...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'HTR1D' 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
Q40.493
Q40
Are there any specific alleles within the gene NLRP7 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Whole Blood and Cortex samples tested, there are no alleles within the gene NLRP7 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 = 'NLRP7' 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
Q40.565
Q40
Are there any specific alleles within the gene CTC-429P9.3 associated with increased susceptibility to developing Amyotrophic Lateral Sclerosis, as determined by significant SMR analysis?
No, based on the Prefrontal Cortex, Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Multi Ancestry Whole Brain, Whole Blood, Whole Brain and Cerebellum samples tested, there are no alleles within the gene CTC-429P9.3 that are significantly associated with an increased susceptibility to developing Amyotrop...
SELECT UUID, Gene, Omic_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-429P9.3' 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
Q40.1151
Q40
Are there any specific alleles within the gene AC010536.1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Caudate Basal Ganglia, Tibial Nerve, Hypothalamus, Liver, Whole Blood and Nucleus Accumbens Basal samples tested, there are no alleles within the gene AC010536.1 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 = 'AC010536.1' 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
Q40.1129
Q40
Are there any specific alleles within the gene C1orf94 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 C1orf94 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 = 'C1orf94' 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
Q40.808
Q40
Are there any specific alleles within the gene ARFGAP3 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Cortex, Prefrontal Cortex, Caudate Basal Ganglia, Tibial Nerve, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Putamen Basal Ganglia and Whole Brain samples tested, there are no alleles within the gene ARFGAP3 that are significantly associated with an increased susceptibility to...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ARFGAP3' 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
Q40.518
Q40
Are there any specific alleles within the gene SHF associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Cerebellum, Spinalcord, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene SHF that are significantly associated with an increased susceptibility to developing Progressive supranucl...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'SHF' 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
Q40.640
Q40
Are there any specific alleles within the gene EMILIN3 associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Hippocampus, Whole Brain, Whole Blood, Cortex, Caudate Basal Ganglia, Multi Ancestry Whole Brain, Hypothalamus, Liver, Putamen Basal Ganglia, Amygdala and Nucleus Accumbens Basal samples tested, there are no alleles within the gene EMILIN3 that are significantly associated with an increased susceptibil...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'EMILIN3' 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
Q40.1480
Q40
Are there any specific alleles within the gene LLGL1 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, Caudate Basal Ganglia, Skeletal Muscle, Hippocampus, Multi Ancestry Whole Brain, Liver, Putamen Basal Ganglia, Cerebellum and Nucleus Accumbens Basal samples tested, there are no alleles within the gene LLGL1 that are significantly associated with an...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'LLGL1' 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
Q40.1789
Q40
Are there any specific alleles within the gene HTR7P1 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
No, based on the Whole Brain, Whole Blood, Prefrontal Cortex, Tibial Nerve, Skeletal Muscle and Hippocampus samples tested, there are no alleles within the gene HTR7P1 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 = 'HTR7P1' 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
Q40.1546
Q40
Are there any specific alleles within the gene EPHB4 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there is 1 allele within the gene EPHB4 that is significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs314320 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.07e-11; b: 4.1119e-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 = 'EPHB4' 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_1495822', 'Gene': 'EPHB4', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs314320', 'A1': 'T', 'A2': 'C', 'Freq': 0.452965, 'p_SMR_multi': 2.072844e-11, 'Disease': 'AD', 'b_SMR': 0.0411192, 'p_HEIDI': 0.1985198}]
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SMR Significance, Effect
Q40.1160
Q40
Are there any specific alleles within the gene SELENOT associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Cortex samples tested, there are no alleles within the gene SELENOT 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 = 'SELENOT' 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
Q40.797
Q40
Are there any specific alleles within the gene MSI1 associated with increased susceptibility to developing Frontotemporal Dementia, 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 MSI1 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 = 'MSI1' 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
Q40.119
Q40
Are there any specific alleles within the gene AP001652.1 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 AP001652.1 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 = 'AP001652.1' 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
Q40.747
Q40
Are there any specific alleles within the gene HAP1 associated with increased susceptibility to developing Lewy Body Dementia, as determined by significant SMR analysis?
No, based on the Whole Blood, Cortex, Tibial Nerve, Multi Ancestry Whole Brain and Whole Brain samples tested, there are no alleles within the gene HAP1 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 = 'HAP1' 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
Q40.1691
Q40
Are there any specific alleles within the gene LINC00658 associated with increased susceptibility to developing Progressive supranuclear palsy, as determined by significant SMR analysis?
No, based on the Whole Blood, Cerebellar Hemisphere and Cerebellum samples tested, there are no alleles within the gene LINC00658 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 = 'LINC00658' 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
Q40.1090
Q40
Are there any specific alleles within the gene LOXL3 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 LOXL3 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 = 'LOXL3' 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
Q40.837
Q40
Are there any specific alleles within the gene OR10J6P associated with increased susceptibility to developing Frontotemporal Dementia, as determined by significant SMR analysis?
No, based on the Liver samples tested, there are no alleles within the gene OR10J6P 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 = 'OR10J6P' 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
Q40.122
Q40
Are there any specific alleles within the gene RARRES1 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
No, based on the Cerebellum, Whole Brain, Whole Blood, Cortex, Frontal Cortex, Cerebellar Hemisphere, Prefrontal Cortex, Tibial Nerve, Multi Ancestry Whole Brain, Hypothalamus and Anterior Cingulate Cortex BA24 samples tested, there are no alleles within the gene RARRES1 that are significantly associated with an increa...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'RARRES1' 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
Q40.663
Q40
Are there any specific alleles within the gene FGF11 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, Skeletal Muscle and Multi Ancestry Whole Brain samples tested, there are no alleles within the gene FGF11 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 = 'FGF11' 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
Q40.1908
Q40
Are there any specific alleles within the gene SDR16C6 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 SDR16C6 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 = 'SDR16C6' 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
Q40.642
Q40
Are there any specific alleles within the gene AC005082.12 associated with increased susceptibility to developing Parkinson's Disease, as determined by significant SMR analysis?
Yes, there are 2 alleles within the gene AC005082.12 that are significantly associated with an increased susceptibility to developing Parkinson's Disease: • rs858295 • Whole Brain: Adjusted SMR multi-SNP P-value: 7.61e-07; b: 2.3425e-01 • rs870476 • Whole Brain: Adjusted SMR multi-SNP P-value: 2.46e-06; b: 1.77...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'AC005082.12' 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_447892', 'Gene': 'AC005082.12', 'Omic_tissue': 'Whole Brain', 'topSNP': 'rs858295', 'A1': 'A', 'A2': 'G', 'Freq': 0.625767, 'p_SMR_multi': 7.614746e-07, 'Disease': 'PD', 'b_SMR': 0.234253, 'p_HEIDI': 0.00494714}, {'UUID': 'NDD_SMR_genes_all_update_text_447891', 'Gene': 'AC005082...
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SMR Significance, Effect
Q40.374
Q40
Are there any specific alleles within the gene MOV10L1 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 and Tibial Nerve samples tested, there are no alleles within the gene MOV10L1 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 = 'MOV10L1' 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
Q40.271
Q40
Are there any specific alleles within the gene APLP1 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 Multi Ancestry Whole Brain samples tested, there are no alleles within the gene APLP1 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 = 'APLP1' 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
Q40.662
Q40
Are there any specific alleles within the gene C1orf229 associated with increased susceptibility to developing Frontotemporal Dementia, 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, Substantia nigra, Hypothalamus, Anterior Cingulate Cortex BA24, Putamen Basal Ganglia, Amygdala, Cerebellum and Nucleus Accumbens Basal samples ...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'C1orf229' 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
Q40.944
Q40
Are there any specific alleles within the gene ZNHIT2 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 ZNHIT2 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 = 'ZNHIT2' 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
Q40.829
Q40
Are there any specific alleles within the gene ABCA7 associated with increased susceptibility to developing Alzheimer's Disease, as determined by significant SMR analysis?
Yes, there are 7 alleles within the gene ABCA7 that are significantly associated with an increased susceptibility to developing Alzheimer's Disease: • rs3764642 • Whole Blood: Adjusted SMR multi-SNP P-value: 2.49e-10; b: 2.3273e-01 • rs2020000 • Whole Blood: Adjusted SMR multi-SNP P-value: 1.32e-08; b: 1.0309e-...
SELECT UUID, Gene, Omic_tissue, topSNP, A1, A2, Freq, p_SMR_multi, Disease, b_SMR, p_HEIDI FROM `{project_id}.{dataset_name}.NeurodegenerativeDiseases_SMR_Genes_Full` WHERE Gene = 'ABCA7' 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_634279', 'Gene': 'ABCA7', 'Omic_tissue': 'Whole Blood', 'topSNP': 'rs3764642', 'A1': 'G', 'A2': 'A', 'Freq': 0.525562, 'p_SMR_multi': 2.490416e-10, 'Disease': 'AD', 'b_SMR': 0.232734, 'p_HEIDI': 0.0002263415}, {'UUID': 'NDD_SMR_genes_all_update_text_634280', 'Gene': 'ABCA7', 'Om...
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SMR Significance, Effect