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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs762513613 0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 11
rs4794067 0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs3827440 0.851 0.120 X 79171491 missense variant T/A;C snv 5.5E-06; 0.51 6
rs3796508 0.827 0.120 4 38828495 missense variant C/T snv 1.2E-02 1.2E-02 6
rs1475539937 0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06 5
rs74315507 0.925 0.080 22 37232857 missense variant C/T snv 4
rs6876739
C7
5 40938240 intron variant T/C snv 0.48 1
rs373495105 19 11507836 missense variant C/A;G;T snv 2.0E-05; 2.8E-05 1
rs1426866722 8 98774764 missense variant C/T snv 7.0E-06 1