{{Rsnum
|rsid=121909748
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFB
|position=31948443
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFB
}}{{omim
|id=138470
|rsnum=121909748
|variant=0006
}}{{ClinVar
|rsid=121909748
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=31916220
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CFB:629
|GENE_NAME=CFB
|GENE_ID=629
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.31916220A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=138470.0006
|CLNSIG=255
|CLNCUI=C2752038; C2752038
|CLNDBN=Atypical hemolytic-uremic syndrome 4
|Disease=Atypical hemolytic-uremic syndrome 4
|CLNACC=RCV000017460.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1367:C2752038:612924:2134
}}