Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs969552874
rs969552874
AMN
C 0.700 GeneticVariation CLINVAR Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. 22929189

2012
dbSNP: rs969552874
rs969552874
AMN
C 0.700 GeneticVariation CLINVAR Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia. 12590260

2003