Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2108622 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs2387326 10 128135192 intergenic variant C/T snv 0.24 2
rs4645543 8 139483999 intergenic variant C/T snv 4.6E-02 1
rs6862909 5 115784737 intergenic variant G/A;T snv 1
rs4852146 2 79397862 intron variant C/T snv 0.71 1