{{Rsnum
|rsid=121434430
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CUBN
|position=17041160
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CUBN
}}{{omim
|id=602997
|rsnum=121434430
|variant=0001
}}{{ClinVar
|rsid=121434430
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=17083159
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=CUBN:8029
|GENE_NAME=CUBN
|GENE_ID=8029
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.17083159G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000007077.1; RCV000049749.1
|CLNDBN=Megaloblastic anemia 1, Finnish type; Megaloblastic anemia due to inborn errors of metabolism
|CLNDSDB=MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1306856:250950:261100:35858:34925000
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602997.0001
|Disease=Megaloblastic anemia 1; Megaloblastic anemia due to inborn errors of metabolism
}}{{PMID Auto
|PMID=22929189
|Title=Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
|OA=1
}}