Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 12
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 10