rs3811647, TF

N. diseases: 15
Disease: Serum transferrin measurement ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Serum transferrin measurement
CUI: C0428545
Disease: Serum transferrin measurement
0.700 GeneticVariation GWASCAT This GWAS, the largest one performed so far in unselected HFE-associated HH (HFE-HH) patients, identified the rs3811647 polymorphism in the TF gene as the only SNP significantly associated with iron metabolism through serum transferrin and iron levels. 25457201 2015
Serum transferrin measurement
CUI: C0428545
Disease: Serum 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