Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35658696
PAM
1.000 0.080 5 103003107 missense variant A/G snv 3.1E-02 3.2E-02 3
rs1456297 15 51672013 regulatory region variant C/A;G;T snv 2