Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs72699866
RIN3
14 92648442 intron variant G/A snv 0.14 4
rs12283755
PPP6R3
11 68604190 intron variant A/G snv 0.24 3
rs4720530
WIPI2
7 5212643 intron variant C/T snv 0.55 3
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 3
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 2
rs10048745
ARHGAP25
2 68735005 5 prime UTR variant G/A snv 0.24 2
rs10901216
FUBP3
9 130596504 intron variant G/A snv 0.28 2
rs118115924
LOC105369757
12 48985754 downstream gene variant G/A;T snv 2
rs12284933
PPP6R3
11 68552021 intron variant G/A snv 0.23 2
rs1262476
LOC105377992
6 126665850 intron variant A/G;T snv 2
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 2
rs13469
POLDIP2
17 28349109 synonymous variant C/G;T snv 0.53 2
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 2
rs1564981 16 50952397 intergenic variant G/A snv 0.60 2
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 2
rs2531992
ADCY9
16 3971733 intron variant A/G snv 0.80 2
rs2955382
GID4
17 18044396 intron variant C/T snv 0.43 2
rs3765350
WNT4
1 22120823 intron variant A/G snv 0.22 2
rs4480845
HIC1
17 2055315 intron variant T/C snv 0.64 2
rs4580892 6 127088737 intron variant C/T snv 0.32 2
rs4980659
LINC01488
11 69484769 intron variant C/A;G snv 2
rs505404
PSMD13
11 243268 non coding transcript exon variant T/G snv 0.28 2