Variant: rs1555381485 

    present in Gene: AMN
    present in Chromosome: 14
    Position on Chromosome: 102929537
    Alleles of this Variant: G/A

rs1555381485 in AMN gene and Megaloblastic Anemia 1 PMID 22929189 2012 Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.

PMID 12590260 2003 Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia.