Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9