rs3811647, TF

N. diseases: 15
Disease: Iron deficiency ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Iron deficiency
CUI: C0240066
Disease: Iron deficiency
0.010 GeneticVariation BEFREE Variants rs3811647 in TF and rs7385804 in TFR2 were associated with reduced SI, serum transferrin and transferrin saturation levels; however, these variants were not associated with iron deficiency or anemia risk. 22323359 2012