{{Rsnum
|rsid=3753395
|Gene=CFH
|Chromosome=1
|position=196717522
|Orientation=plus
|GMAF=0.4582
|Gene_s=CFH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 38.5 | 41.5 | 20.0
| HCB | 35.6 | 42.2 | 22.2
| JPT | 34.1 | 52.3 | 13.6
| YRI | 9.5 | 49.2 | 41.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 35.6 | 42.2 | 22.2
| 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
}}{{PMID Auto
|PMID=23423485
|Title=Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China
}}

{{PMID Auto
|PMID=16936733
|Title=CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.
|OA=1
}}

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