SLC40A1, solute carrier family 40 member 1, 30061

N. diseases: 101; N. variants: 31
Disease: Anemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11568350
rs11568350
Entrez Id: 30061
Gene Symbol: SLC40A1
SLC40A1
CUI: C0002871
Disease:
Anemia 		0.010 GeneticVariation BEFREE We conclude that the Q248H mutation is a common polymorphism in the ferroportin 1 gene in African populations that may be associated with mild anemia and a tendency to iron loading. 14636642 2004