Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs16851720 0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4