{{Rsnum
|rsid=80338699
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CDAN1
|position=42725550
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CDAN1
}}{{omim
|id=607465
|rsnum=80338699
|variant=0002
}}{{ClinVar
|rsid=80338699
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=43017748
|CHROM=15
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=CDAN1:146059
|GENE_NAME=CDAN1
|GENE_ID=146059
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.43017748G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK5313; 607465.0002
|CLNSIG=5
|CLNCUI=C0271933
|CLNDBN=Congenital dyserythropoietic anemia, type I
|Disease=Congenital dyserythropoietic anemia
|CLNACC=RCV000020959.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK5313:C0271933:224120:98869:59548005
}}{{PMID Auto
|PMID=12434312
|Title=Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
|OA=1
}}