Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 79
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 10
rs7904519 0.763 0.240 10 113014168 intron variant A/G snv 0.55 8