SLC40A1, solute carrier family 40 member 1, 30061

N. diseases: 101; N. variants: 31
Disease: Hemochromatosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893662
rs104893662
Entrez Id: 30061
Gene Symbol: SLC40A1
SLC40A1
CUI: C0018995
Disease:
Hemochromatosis 		0.010 GeneticVariation BEFREE Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristics. 12547233 2003