{{Rsnum
|rsid=121913053
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFH
|position=196740712
|Gene_s=CFH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134370
|rsnum=121913053
|variant=0003
}}{{ClinVar
|rsid=121913053
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=196740712
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260080a05000002110100
|GENEINFO=CFH:3075
|GENE_NAME=CFH
|GENE_ID=3075
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.196740712G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000186.3:c.2876G>A; 134370.0003
|CLNSIG=5
|CLNCUI=C0398777
|CLNDBN=Factor H deficiency
|Disease=Factor H deficiency
|CLNACC=RCV000018010.26
|Tags=PM;S3D;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1425:C0398777:609814:234622003
}}