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
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs2834167 0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 11
rs1800451 0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs1801690 0.925 0.120 17 66212167 missense variant C/G snv 4.8E-02 4.0E-02 6
rs11552708 0.882 0.240 17 7559238 missense variant G/A;C snv 0.13; 4.2E-06 5