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
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
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
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15