{{Rsnum
|rsid=386834172
|Chromosome=14
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=AMN
|position=102922732
|Gene_s=AMN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000050166.1
|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.103389069G>T
|CLNSIG=4
|Disease=Megaloblastic anemia due to inborn errors of metabolism
|FwdALT=T
|FwdREF=G
|REF=G
|RSPOS=103389069
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386834172
|GENEINFO=AMN:81693
|GENE_ID=81693
|GENE_NAME=AMN
}}{{PMID Auto
|PMID=18181028
|Title=Amnionless (AMN) mutations in Imerslund-Grasbeck syndrome may be associated with disturbed vitamin B(12) transport into the CNS.
}}