Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2979489 8 30423317 intron variant G/A;C snv 6
rs35091702 8 30421955 intron variant GAAAAAA/- delins 0.78 2
rs2915607 8 30422400 intron variant T/C snv 0.80 1