Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs1989839 0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8