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 19
rs11196170 0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 9