TFR2, transferrin receptor 2, 7036

N. diseases: 92; N. variants: 50
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement
0.100 GeneticVariation phenotype GWASCAT Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. 25352340 2014
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement
0.100 GeneticVariation phenotype GWASCAT Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. 21208937 2011