Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6570507 0.827 0.240 6 142358435 intron variant G/A snv 0.47 11
rs11205303 0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs7741741 0.925 0.040 6 142334664 intron variant T/A;G snv 6
rs10739217 0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3