{{Rsnum
|rsid=121909585
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=C3
|position=6692971
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C3
}}{{omim
|id=120700
|rsnum=121909585
|variant=0007
}}{{ClinVar
|rsid=121909585
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=6692982
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=C3:718
|GENE_NAME=C3
|GENE_ID=718
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.6692982C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120700.0007
|CLNSIG=255
|CLNCUI=C2752037
|CLNDBN=Atypical hemolytic-uremic syndrome 5
|Disease=Atypical hemolytic-uremic syndrome 5
|CLNACC=RCV000018591.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1367:C2752037:612925:2134
}}