Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213