Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 11
rs7013278 0.776 0.080 8 127402647 intron variant T/C snv 0.59 10
rs7014346 0.732 0.240 8 127412547 intron variant A/G snv 0.63 9
rs12682374 0.790 0.080 8 127398703 intron variant C/A;G;T snv 9