{{Rsnum
|rsid=121917784
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FANCC
|position=95249255
|Gene_s=FANCC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=227645
|rsnum=121917784
|variant=0004
}}{{ClinVar
|rsid=121917784
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=98011537
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FANCC:2176
|GENE_NAME=FANCC
|GENE_ID=2176
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.98011537G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1401; 613899.0004
|CLNSIG=5
|CLNCUI=CN069621
|CLNDBN=Fanconi anemia, complementation group C
|Disease=Fanconi anemia
|CLNACC=RCV000012826.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1401:C3468041:227645:84
}}