Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs6967330 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 8