Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs55705857 0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16