Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11563582 7 27312031 intergenic variant G/A snv 9.8E-02 3
rs1173766 5 32804422 intergenic variant T/C snv 0.57 3
rs11953630 5 158418394 intergenic variant C/A;T snv 3
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs4373814 10 18131043 intergenic variant G/C;T snv 3
rs4462906 3 27551369 upstream gene variant T/A;G snv 3
rs6712094 2 164186950 intron variant A/G snv 0.23 3
rs6871087 0.925 0.040 5 30899410 intergenic variant A/G snv 8.5E-02 3
rs7006531 8 94098516 intron variant A/C;G snv 3
rs7690819 1.000 0.040 4 111199502 intergenic variant A/G;T snv 3
rs820430 3 27507409 regulatory region variant A/G snv 0.30 3
rs9385284 6 123078960 intergenic variant A/G snv 0.24 3
rs28868104 1.000 0.080 3 104241993 intergenic variant C/T snv 0.17 2
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs10069554 5 33204354 intron variant T/C snv 0.45 1
rs10279895 7 27288591 intergenic variant A/G snv 2.9E-02 1
rs11020821 11 94538497 intergenic variant C/A snv 0.28 1
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 1
rs145054295 11 96709521 intron variant AT/- del 7.0E-03 1
rs180912 10 113982069 regulatory region variant T/G snv 0.56 1
rs2469997 8 119341027 intergenic variant G/C snv 0.83 1
rs2820037 1.000 0.040 1 239273242 intergenic variant A/T snv 0.21 1
rs35434 12 115116871 intergenic variant G/A snv 0.22 1
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 1