{{Rsnum
|rsid=182512508
|Gene=CUBN
|Chromosome=10
|position=17085756
|Orientation=plus
|GMAF=0.002755
|Gene_s=CUBN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=A,C
|CAF=0.9972; 0.002755
|CHROM=10
|CLNACC=RCV000049736.1
|CLNALLE=1
|CLNDBN=Megaloblastic anemia due to inborn errors of metabolism
|CLNDSDB=MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1306856:250950:261100:35858:34925000
|CLNHGVS=NC_000010.10:g.17127755G>A
|CLNSIG=4
|COMMON=1
|Disease=Megaloblastic anemia due to inborn errors of metabolism
|FwdALT=A,C
|FwdREF=G
|GENEINFO=CUBN:8029
|GENE_ID=8029
|GENE_NAME=CUBN
|REF=G
|RSPOS=17127755
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268000000000416110100
|WGT=0
|dbSNPBuildID=135
|rsid=182512508
}}{{PMID Auto
|PMID=15024727
|Title=Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.
}}