rs3811647, TF

N. diseases: 15
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Transferrin measurement
CUI: C0202105
Disease: Transferrin measurement
0.700 GeneticVariation GWASCAT Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. 25457201 2015
Transferrin measurement
CUI: C0202105
Disease: Transferrin measurement
0.700 GeneticVariation GWASCAT Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. 21208937 2011