Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3731217 0.763 0.320 9 21984662 intron variant A/C;T snv 1
rs3731249 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 1