Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48