{{Rsnum
|rsid=2284664
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=1
|Orientation=minus
|Gene=CFH
|position=196733395
|Gene_s=CFH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.5 | 28.2 | 66.4
| HCB | 8.8 | 40.4 | 50.7
| JPT | 18.8 | 43.8 | 37.5
| YRI | 0.7 | 9.6 | 89.7
| ASW | 1.8 | 15.8 | 82.5
| CHB | 8.8 | 40.4 | 50.7
| CHD | 17.4 | 34.9 | 47.7
| GIH | 0.0 | 28.7 | 71.3
| LWK | 0.0 | 6.4 | 93.6
| MEX | 8.9 | 41.1 | 50.0
| MKK | 0.0 | 12.2 | 87.8
| TSI | 3.9 | 39.2 | 56.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=24365176
|Title=Common variants in the complement factor H gene confer genetic susceptibility to central serous chorioretinopathy
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}