{{Rsnum
|rsid=203674
|Gene=CFH
|Chromosome=1
|position=196715495
|Orientation=minus
|GMAF=0.2576
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CFH
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 33.0 | 51.8 | 15.2
| HCB | 84.7 | 14.6 | 0.7
| JPT | 90.3 | 8.8 | 0.9
| YRI | 63.2 | 34.7 | 2.1
| ASW | 56.1 | 33.3 | 10.5
| CHB | 84.7 | 14.6 | 0.7
| CHD | 95.4 | 4.6 | 0.0
| GIH | 43.0 | 46.0 | 11.0
| LWK | 63.3 | 33.9 | 2.8
| MEX | 52.6 | 38.6 | 8.8
| MKK | 61.7 | 31.8 | 6.5
| TSI | 46.1 | 36.3 | 17.6
| HapMapRevision=28
}}
[[age related macular degeneration]] {{PMID|15870199|OA=1
}}

{{PMID Auto
|PMID=18043728
|Title=Haplotypes in the complement factor H (CFH) gene: associations with drusen and advanced age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=18541031
|Title=The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}