Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1635852 0.882 0.160 7 28149792 intron variant T/C snv 0.42 2
rs1029534 7 28149464 intron variant T/C;G snv 1
rs1708299 7 28150327 intron variant A/G snv 0.77 1
rs849141 0.851 0.240 7 28145472 intron variant A/G snv 0.78 1