Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 5
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs72699866
RIN3
14 92648442 intron variant G/A snv 0.14 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 3
rs12283755
PPP6R3
11 68604190 intron variant A/G snv 0.24 3
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 3
rs4720530
WIPI2
7 5212643 intron variant C/T snv 0.55 3
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 3
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 2
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs1564981 16 50952397 intergenic variant G/A snv 0.60 2
rs3018362 0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67 2
rs4580892 6 127088737 intron variant C/T snv 0.32 2
rs6726821 2 165721604 intergenic variant T/G snv 0.40 2
rs6959212 7 38088724 intergenic variant T/C;G snv 2
rs7672749 4 87877132 intergenic variant G/A snv 0.11 2
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 2
rs2531992
ADCY9
16 3971733 intron variant A/G snv 0.80 2
rs10048745
ARHGAP25
2 68735005 5 prime UTR variant G/A snv 0.24 2