Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs3918226 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs13108218 4 3442204 intron variant A/G;T snv 7
rs114165349 1 26695422 intron variant G/C snv 1.7E-02 5
rs9292468 5 32818967 intergenic variant T/A;C snv 5