Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1033180 1.000 0.080 6 383546 regulatory region variant C/T snv 5.4E-02 1
rs10886159 1.000 0.080 10 117854099 intergenic variant T/C snv 0.25 1
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 1
rs12142280 1.000 0.080 1 172895512 intron variant T/A snv 0.21 1
rs12727642 1.000 0.080 1 7986612 upstream gene variant C/A snv 0.12 1
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 1
rs1378938 1.000 0.080 15 74804102 downstream gene variant T/A;C snv 1
rs2097282 1.000 0.080 3 46336534 intergenic variant C/T snv 0.68 1
rs2157453 1.000 0.080 1 172894808 intron variant G/A snv 0.31 1
rs2187670 1.000 0.080 3 46325463 intergenic variant T/C snv 0.81 1
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 1
rs424232 0.882 0.240 6 32240547 intergenic variant C/A;T snv 1
rs4558075 1.000 0.080 10 6359663 intergenic variant C/A;G;T snv 1
rs4899260 1.000 0.080 14 68811487 intergenic variant C/T snv 0.28 1
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 1
rs62184863 1.000 0.080 2 203819074 intergenic variant G/C snv 6.2E-02 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 1
rs7104791 1.000 0.080 11 111326133 downstream gene variant T/A;C snv 1
rs859715 1.000 0.080 1 172790982 intron variant A/T snv 0.36 1
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 1
rs971290 1.000 0.080 14 68805252 intergenic variant C/A;G;T snv 1
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 1
rs8081319
ACACA ; C17orf78
1.000 0.080 17 37374139 intron variant A/G snv 6.8E-02 1
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 1
rs61579022
ARHGAP31
1.000 0.080 3 119404431 intron variant G/A snv 0.30 1