{{Rsnum
|rsid=121909589
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CD46
|position=207767057
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CD46
}}{{omim
|id=120920
|rsnum=121909589
|variant=0003
}}{{ClinVar
|rsid=121909589
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=207767057
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=CD46:4179
|GENE_NAME=CD46
|GENE_ID=4179
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.207767057T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_002389.4:c.718T>C; 120920.0003
|CLNSIG=255
|CLNCUI=C2752040
|CLNDBN=Atypical hemolytic-uremic syndrome 2
|Disease=Atypical hemolytic-uremic syndrome 2
|CLNACC=RCV000018574.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1367:C2752040:612922:ORPHA2134
}}