Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51