Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs702873 0.882 0.120 2 60854407 intron variant C/T snv 0.35 3
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 2
rs33980500 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 2