{{Rsnum
|rsid=386834170
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=AMN
|position=102928424
|Gene_s=AMN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=14
|CLNACC=RCV000050164.1
|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.103394761A>G
|CLNSIG=4
|Disease=Megaloblastic anemia due to inborn errors of metabolism
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=103394761
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386834170
|GENEINFO=AMN:81693
|GENE_ID=81693
|GENE_NAME=AMN
}}{{PMID Auto
|PMID=12590260
|Title=Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia.
}}

{{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.
}}

{{PMID Auto
|PMID=17114957
|Title=Imerslund-Grasbeck syndrome associated with recurrent aphthous stomatitis and defective neutrophil function.
}}

{{PMID Auto
|PMID=17285242
|Title=Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients.
}}

{{PMID Auto
|PMID=22078000
|Title=Ancient founder mutation is responsible for Imerslund-Grasbeck Syndrome among diverse ethnicities.
|OA=1
}}