rs104893662, SLC40A1

N. diseases: 4
Disease: Hemochromatosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
0.010 GeneticVariation BEFREE Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristics. 12547233 2003