TF, transferrin, 7018

N. diseases: 168; N. variants: 74
Disease: Transferrin measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3811647
rs3811647
Entrez Id: 7018
Gene Symbol: TF
TF
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
dbSNP: rs8177179
rs8177179
Entrez Id: 7018;100129696
Gene Symbol: TF;INHCAP
TF;INHCAP
CUI: C0202105
Disease:
Transferrin measurement 		A 0.700 GeneticVariation GWASCAT Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. 25352340 2014
dbSNP: rs8177240
rs8177240
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0202105
Disease:
Transferrin measurement 		T 0.700 GeneticVariation GWASCAT Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. 25352340 2014
dbSNP: rs3811647
rs3811647
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0202105
Disease:
Transferrin measurement 		A 0.700 GeneticVariation GWASCAT Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. 21208937 2011