{{Rsnum
|rsid=1048709
|Gene=CFB
|Chromosome=6
|position=31947158
|Orientation=plus
|GMAF=0.174
|Gene_s=CFB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.3 | 35.4 | 59.3
| HCB | 8.0 | 46.0 | 46.0
| JPT | 6.2 | 44.2 | 49.6
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 7.0 | 93.0
| CHB | 8.0 | 46.0 | 46.0
| CHD | 6.4 | 50.5 | 43.1
| GIH | 1.0 | 24.8 | 74.3
| LWK | 0.0 | 5.5 | 94.5
| MEX | 1.7 | 31.0 | 67.2
| MKK | 0.0 | 3.2 | 96.8
| TSI | 1.0 | 19.6 | 79.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=23864767
|Title=Association of CFH and CFB gene polymorphisms with retinopathy in type 2 diabetic patients
|OA=1
}}

{{PMID Auto
|PMID=18806293
|Title=Analysis of rare variants in the complement component 2 (C2) and factor B (BF) genes refine association for age-related macular degeneration (AMD).
}}

{{PMID Auto
|PMID=22714898
|Title=Association of C2 and CFB polymorphisms with anterior uveitis.
}}

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