Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
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
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151