Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 40
rs11554137 0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13