Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 18