Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs121913238 0.732 0.240 12 25227343 missense variant G/C;T snv 17