Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246