Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs10795668 0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17