TF, transferrin, 7018

N. diseases: 168; N. variants: 74
Disease: Serum transferrin measurement ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. 25457201 2015
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		0.100 GeneticVariation phenotype GWASCAT Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. 25352340 2014
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin 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