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PheGenI_Association.tab
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PheGenI_Association.tab
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# Trait SNP rs Context Gene Gene ID Gene 2 Gene ID 2 Chromosome Location P-Value Source PubMed Analysis ID Study ID Study Name Population
1 Parkinson Disease 356182 intergenic GPRIN3 285513 SNCA 6622 4 89704960 4E-73 NHGRI 25064009 European
2 Parkinson Disease 356219 intergenic GPRIN3 285513 SNCA 6622 4 89716450 6E-65 NHGRI 22438815 Asian|European
3 Parkinson Disease 356182 intergenic GPRIN3 285513 SNCA 6622 4 89704960 1E-56 NHGRI 27182965 European
4 Parkinson Disease 356219 intergenic GPRIN3 285513 SNCA 6622 4 89716450 2E-47 NHGRI 21292315 European
5 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 8E-35 NHGRI 22451204 European
6 Parkinson Disease 8180209 intergenic GPRIN3 285513 SNCA 6622 4 89723303 1E-32 NHGRI 28011712 East Asian
7 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 2E-19 NHGRI 21738487 European
8 Parkinson Disease 11931074 intergenic GPRIN3 285513 SNCA 6622 4 89718364 7E-17 NHGRI 19915576 East Asian|European
9 Parkinson Disease 2736990 intron SNCA 6622 SNCA 6622 4 89757390 2E-16 NHGRI 19915575 European
10 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 9E-16 NHGRI 21044948 European
11 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 3E-11 NHGRI 20711177 European
12 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 3E-11 NHGRI 24511991 European
13 Parkinson Disease 6532194 intergenic SNCA 6622 MMRN1 22915 4 89859751 5E-11 NHGRI 22438815 Asian|European
14 C-Reactive Protein 3775442 intron SNCA 6622 SNCA 6622 4 89794080 3.21432866712515E-10 dbGaP 17903293 1134 342 NHLBI Framingham SNP Health Association Resource (SHARe) European
15 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 1E-9 NHGRI 24511991 European
16 Parkinson Disease 2736990 intron SNCA 6622 SNCA 6622 4 89757390 5.69E-9 dbGaP 19915575 2868 89 NINDS- Genome-Wide Genotyping in Parkinson's Disease European
17 C-Reactive Protein 3857060 intron SNCA 6622 SNCA 6622 4 89758377 6.95974558227867E-9 dbGaP 17903293 1134 342 NHLBI Framingham SNP Health Association Resource (SHARe) European
18 Platelet Function Tests 11728943 intergenic GPRIN3 285513 SNCA 6622 4 89623888 1.6900000E-008 dbGaP 0 3143 375 Genome-Wide Association of Platelet Phenotypes African American
19 Bupropion 1908557 intergenic GPRIN3 285513 SNCA 6622 4 89500202 3E-8 NHGRI 27622933 European
20 Depressive Disorder 1908557 intergenic GPRIN3 285513 SNCA 6622 4 89500202 3E-8 NHGRI 27622933 European
21 Mood Disorders 1908557 intergenic GPRIN3 285513 SNCA 6622 4 89500202 3E-8 NHGRI 27622933 European
22 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 3E-8 NHGRI 21084426 European
23 Parkinson Disease 3857059 intron SNCA 6622 SNCA 6622 4 89754087 3.6E-8 dbGaP 19915575 2868 89 NINDS- Genome-Wide Genotyping in Parkinson's Disease European
24 Parkinson Disease 11931074 intergenic GPRIN3 285513 SNCA 6622 4 89718364 4.78E-8 dbGaP 19915575 2868 89 NINDS- Genome-Wide Genotyping in Parkinson's Disease European
25 Parkinson Disease 356220 intergenic GPRIN3 285513 SNCA 6622 4 89720189 6.99E-8 dbGaP 19915575 2868 89 NINDS- Genome-Wide Genotyping in Parkinson's Disease European
26 Parkinson Disease 2736990 intron SNCA 6622 SNCA 6622 4 89757390 7E-8 NHGRI 20070850 European
27 Parkinson Disease 6532197 intergenic SNCA 6622 MMRN1 22915 4 89876150 1E-7 NHGRI 19915575 European
28 Hip 10516842 intergenic GPRIN3 285513 SNCA 6622 4 89685029 1.07499466014977E-6 dbGaP 17903296 1826 342 NHLBI Framingham SNP Health Association Resource (SHARe) European
29 Neuroticism 1372520 intron SNCA 6622 SNCA 6622 4 89836354 2E-6 NHGRI 27089181 European
30 Coronary Disease 356228 intergenic GPRIN3 285513 SNCA 6622 4 89685975 3.1810000E-006 dbGaP 0 3910 930 CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology) European
31 Parkinson Disease 3775439 intron SNCA 6622 SNCA 6622 4 89788590 4.43E-6 dbGaP 19915575 2868 89 NINDS- Genome-Wide Genotyping in Parkinson's Disease European
32 Cytokine Receptor gp130 356191 intron SNCA 6622 SNCA 6622 4 89766969 2.0930000E-005 dbGaP 0 3748 215 Genome-Wide Association Analysis of Biomarkers in the InCHIANTI and BLSA European
33 Cytokine Receptor gp130 356188 intron SNCA 6622 SNCA 6622 4 89770386 2.1120000E-005 dbGaP 0 3748 215 Genome-Wide Association Analysis of Biomarkers in the InCHIANTI and BLSA European
34 Parkinson Disease 12644119 intergenic GPRIN3 285513 SNCA 6622 4 89682268 2.15E-5 dbGaP 19915575 2868 89 NINDS- Genome-Wide Genotyping in Parkinson's Disease European
35 Cytokine Receptor gp130 2583978 intron SNCA 6622 SNCA 6622 4 89829175 2.4690000E-005 dbGaP 0 3748 215 Genome-Wide Association Analysis of Biomarkers in the InCHIANTI and BLSA European
36 Parkinson Disease 894278 intron SNCA 6622 SNCA 6622 4 89813384 2.64E-5 dbGaP 19915575 2868 89 NINDS- Genome-Wide Genotyping in Parkinson's Disease European
37 Cytokine Receptor gp130 2197120 intron SNCA 6622 SNCA 6622 4 89808451 2.7960000E-005 dbGaP 0 3748 215 Genome-Wide Association Analysis of Biomarkers in the InCHIANTI and BLSA European
38 C-Reactive Protein 7678651 intergenic SNCA 6622 MMRN1 22915 4 89847220 5.09992075077292E-5 dbGaP 17903293 1131 342 NHLBI Framingham SNP Health Association Resource (SHARe) European
39 Parkinson Disease 356229 intergenic GPRIN3 285513 SNCA 6622 4 89685446 5.48E-5 dbGaP 21829596 2865 126 CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) European
40 Alcoholism 6532194 intergenic SNCA 6622 MMRN1 22915 4 89859751 8.29928e-005 dbGaP 22978509 2906 92 Study of Addiction: Genetics and Environment (SAGE) European
41 Parkinson Disease 356188 intron SNCA 6622 SNCA 6622 4 89770386 8.41E-5 dbGaP 21829596 2865 126 CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) European
42 Parkinson Disease 1504489 intergenic GPRIN3 285513 SNCA 6622 4 89337437 8.42E-5 dbGaP 21829596 2865 126 CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) European
43 Parkinson Disease 4106153 intergenic GPRIN3 285513 SNCA 6622 4 89323325 9.18E-5 dbGaP 21829596 2865 126 CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) European
44 Myocardial Infarction 1473533 intergenic GPRIN3 285513 SNCA 6622 4 89595528 3.8409762E-004 dbGaP 0 2883 226 STAMPEED: Cardiovascular Health Study (CHS) African American