Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147