Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs11175593
LRRK2 ; LRRK2-DT ; LINC02471 ; LOC105369735
0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 3
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 3
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs1551398
LOC105375746
0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3