Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 27
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 16