Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 7
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2523578 1.000 6 31360765 upstream gene variant G/A snv 0.79 5
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs295301 0.851 0.160 3 141619799 downstream gene variant G/A snv 0.38 5
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 5
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 4
rs1173727 5 32830415 intergenic variant T/C snv 0.66 4
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 4
rs1490384 6 126530014 intron variant C/G;T snv 4
rs1776897 6 34227234 regulatory region variant G/T snv 0.80 4
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 4
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs6959212 7 38088724 intergenic variant T/C;G snv 4
rs74929147 19 18302251 downstream gene variant G/A;C snv 4