Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11681351 0.925 0.120 2 27520556 intron variant G/A snv 0.36 3
rs13472 0.925 0.120 2 27377372 3 prime UTR variant G/A snv 0.38 3
rs2293572 0.925 0.120 2 27505910 intron variant C/G snv 0.39 3
rs4665963 0.925 0.120 2 27305824 splice region variant T/C snv 0.35 0.43 3
rs1528533 0.925 0.120 2 27372889 non coding transcript exon variant G/C snv 0.47 3
rs813592 0.925 0.120 2 27499104 intron variant T/C snv 0.42 0.47 3
rs1049817 0.925 0.120 2 27328100 synonymous variant A/G snv 0.42 0.48 3
rs7586601 0.925 0.120 2 27361799 intron variant A/G snv 0.54 3
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13