Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs1805008 0.732 0.240 16 89919736 missense variant C/T snv 4.7E-02 4.8E-02 16