Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs10877012 0.763 0.280 12 57768302 intron variant G/C;T snv 10