{{Rsnum
|rsid=121913057
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CFH
|position=196737575
|Gene_s=CFH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134370
|rsnum=121913057
|variant=0012
}}{{ClinVar
|rsid=121913057
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=196737575
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260080605000002110100
|GENEINFO=CFH:3075
|GENE_NAME=CFH
|GENE_ID=3075
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.196737575T>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000186.3:c.2697T>A; 134370.0012
|CLNSIG=255
|CLNCUI=C1856142
|CLNDBN=Atypical hemolytic-uremic syndrome 1
|Disease=Atypical hemolytic-uremic syndrome 1
|CLNACC=RCV000018020.1
|Tags=PM;S3D;NSN;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1367:C2749604:235400:ORPHA2134
}}