{{Rsnum
|rsid=529825
|Gene=CFH
|Chromosome=1
|position=196665976
|Orientation=minus
|GMAF=0.4284
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CFH
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 67.7 | 27.7 | 4.6
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
[[age related macular degeneration]] {{PMID|15870199|OA=1
}}

{{PMID Auto
|PMID=21882633
|Title=[Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 1: The impact of CFH and IL-8 genes polymorphism]
}}

{{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=18787502
|Title=Genetic contributions to the development of retinopathy of prematurity.
|OA=1
}}

{{PMID Auto
|PMID=19861685
|Title=Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.
|OA=1
}}

{{PMID Auto
|PMID=20378180
|Title=Three major loci involved in age-related macular degeneration are also associated with polypoidal choroidal vasculopathy.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}