Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3024493 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 2
rs3024490 0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 1
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1