Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs7014346 0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
rs540635787 0.851 0.200 22 28694073 missense variant G/A;C;T snv 1.7E-05 4
rs7837328 0.882 0.120 8 127410882 intron variant A/G snv 0.52 2