{{Rsnum
|rsid = 460897
|Gene = CFH
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=1
|position=196747189
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFH
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 100.0
| 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
}}
{{omim
|desc=HEMOLYTIC UREMIC SYNDROME, ATYPICAL
|id=134370
|rsnum=460897
|variant=0004
}}
{{ neighbor
| rsid = 28929497
| distance = 48
}}

{{ClinVar
|rsid=460897
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=196747189
|CHROM=1
|dbSNPBuildID=80
|SSR=1
|SAO=1
|VP=0x050368000a05070103110140
|GENEINFO=CFH:3075
|GENE_NAME=CFH
|GENE_ID=3075
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.196747189C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000186.3:c.3572C>T; NBK1367; 134370.0004
|CLNSIG=255
|CLNCUI=C1856142; C1856142
|CLNDBN=Atypical hemolytic-uremic syndrome 1
|Disease=Atypical hemolytic-uremic syndrome 1
|CLNACC=RCV000018011.2
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;VLD;G5A;G5;GNO;OTHERKG;PH3;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1367:C2749604:235400:ORPHA2134
}}

{{PMID Auto
|PMID=9811382
|Title=Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H.
}}

{{PMID Auto
|PMID=10577907
|Title=Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
|OA=1
}}

{{PMID Auto
|PMID=10762557
|Title=Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
|OA=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
}}

{{on chip | 23andMe v3}}