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
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21