Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs2075820 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs397514767 0.807 0.240 11 33710247 missense variant C/T snv 4.0E-06 7
rs1445335859 0.851 0.240 X 15331662 missense variant T/C snv 9.4E-06 5
rs1253159682 1.000 0.080 1 158255333 missense variant A/G snv 7.0E-06 1
rs746073437 1.000 0.080 1 158356780 missense variant G/C snv 4.0E-06 1
rs762142186 1.000 0.080 1 161624600 missense variant C/G;T snv 4.0E-06 1