rs104893662, SLC40A1

N. diseases: 4
Disease: Iron Overload ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Iron Overload
CUI: C0282193
Disease: Iron Overload
0.010 GeneticVariation BEFREE We describe here the clinical and biological characteristics of autosomal dominant form of iron overload due to the N144H mutation of the SLC11A3 gene. 12547233 2003