Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs6910071 0.790 0.320 6 32315077 intron variant A/G snv 0.14 7
rs6906021 0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 6