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
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19