Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24