Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519919 0.851 0.160 2 15942195 missense variant C/T snv 5