{{Rsnum
|rsid=460184
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFH
|position=196747207
|Gene_s=CFH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 95.4 | 4.6 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 77.0 | 23.0 | 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
}}{{ClinVar
|rsid=460184
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=196747207
|CHROM=1
|dbSNPBuildID=80
|SSR=1
|SAO=1
|VP=0x050368000a05050103110140
|GENEINFO=CFH:3075
|GENE_NAME=CFH
|GENE_ID=3075
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.196747207T>C
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=235400
|CLNDBN=Atypical hemolytic-uremic syndrome 1
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;VLD;G5;GNO;OTHERKG;PH3;LSD;OM
|CLNACC=RCV000020180.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1367:C2749604:235400:ORPHA2134
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_000186.3:c.3590T>C; NBK1367
|Disease=Atypical hemolytic-uremic syndrome 1
}}{{PMID Auto
|PMID=16470555
|Title=De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.
}}

{{PMID Auto
|PMID=17076561
|Title=Atypical haemolytic uraemic syndrome associated with a hybrid complement gene.
|OA=1
}}