Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs121434491 0.752 0.200 2 55871091 missense variant G/A snv 15
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 10
rs61750200 0.790 0.080 1 94098928 missense variant G/A;T snv 1.1E-04; 8.0E-06 8
rs201471607 0.851 0.080 1 94046943 missense variant T/C snv 1.4E-04 7.7E-05 7
rs61751392 0.827 0.080 1 94063250 missense variant A/G snv 1.5E-04 1.7E-04 7
rs62645944 0.807 0.080 1 94098794 splice region variant C/A snv 8.8E-05 6.3E-05 7
rs76157638 0.851 0.080 1 94051698 missense variant C/G;T snv 4.4E-03; 4.0E-06 6
rs61751408 0.851 0.080 1 94005509 missense variant G/A snv 2.0E-04 1.7E-04 5
rs28938473 0.882 0.040 1 94007731 missense variant G/A snv 3.0E-03 3.6E-03 4
rs61750120 0.882 0.160 1 94042767 missense variant G/A snv 1.2E-04 1.8E-04 4
rs61751407 0.882 0.080 1 94010795 splice region variant C/A;T snv 3.1E-04 3.5E-04 4
rs61753033 0.882 0.080 1 94008767 missense variant A/G snv 2.0E-05 4
rs1801466 1.000 1 94010911 missense variant T/A snv 4.3E-02 4.1E-02 3
rs61750138 1.000 1 94030991 splice region variant C/A;T snv 1.2E-05 3
rs121909205 1.000 1 94120994 missense variant G/A;T snv 1.6E-05; 3.6E-05 2
rs150774447 1.000 1 94111579 missense variant C/A;T snv 4.0E-06; 2.4E-05 2
rs3112831 1.000 0.080 1 94078678 missense variant T/C;G snv 0.26 0.26 2
rs61753034 1.000 1 94007727 missense variant A/C snv 2
rs756840095 1.000 1 94042797 missense variant G/A snv 2.4E-05 6.3E-05 2
rs760549861 1.000 1 94014685 missense variant G/A snv 7.6E-05 7.0E-06 2
rs775179967 1.000 6 38791670 missense variant A/G snv 1.2E-05 1.4E-05 2
rs137853300 1.000 0.040 22 32859277 missense variant C/G snv 2