{{Rsnum
|rsid=386834173
|Chromosome=14
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=AMN
|position=102928930
|Gene_s=AMN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CT
|CHROM=14
|CLNACC=RCV000050167.1
|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_000014.8:g.103395267dupT
|CLNSIG=4
|Disease=Megaloblastic anemia due to inborn errors of metabolism
|FwdALT=T
|REF=C
|RSPOS=103395266
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386834173
|GENEINFO=AMN:81693
|GENE_ID=81693
|GENE_NAME=AMN
}}{{PMID Auto
|PMID=22929189
|Title=Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
|OA=1
}}