Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs1131691029 0.827 0.160 17 7673794 missense variant C/G snv 6
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
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
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147