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
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23