Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6