Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs12927355 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 2