Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs121918394 0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5