{{Rsnum
|rsid=386834165
|Chromosome=14
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=AMN
|position=102930489
|Gene_s=AMN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GA
|CHROM=14
|CLNACC=RCV000050159.1
|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.103396826dupA
|CLNSIG=4
|Disease=Megaloblastic anemia due to inborn errors of metabolism
|FwdALT=A
|REF=G
|RSPOS=103396825
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386834165
|GENEINFO=AMN:81693
|GENE_ID=81693
|GENE_NAME=AMN
}}{{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.
}}