Variant: rs3811647 

    present in Gene: TF
    present in Chromosome: 3
    Position on Chromosome: 133765185
    Alleles of this Variant: G/A

rs3811647 in TF gene and Alcohol consumption PMID 21665994 2011 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.

rs3811647 in TF gene and HEMOCHROMATOSIS, TYPE 1 PMID 25457201 2015 Because these two outcomes were clearly associated with the biochemical and clinical expression of the disease, an indirect link between the rs3811647 polymorphism and the phenotypic presentation of HFE-HH is likely.

rs3811647 in TF gene and HFE-Associated Hereditary Hemochromatosis PMID 25457201 2015 Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.

rs3811647 in TF gene and Hereditary hemochromatosis PMID 25457201 2015 Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.

rs3811647 in TF gene and Iron Metabolism Disorders PMID 25457201 2015 Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.

rs3811647 in TF gene and Iron binding capacity total measurement PMID 21483845 2011 An association between total iron binding capacity and SNP rs3811647 in the TF gene (GWAS observed P=7.0×10(-9), corrected P=0.012) was replicated within the VA samples (observed P=0.012).

rs3811647 in TF gene and Iron level result PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

rs3811647 in TF gene and Iron measurement PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

rs3811647 in TF gene and Serum iron measurement PMID 25457201 2015 Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.

rs3811647 in TF gene and Serum transferrin measurement PMID 25457201 2015 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.

PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

rs3811647 in TF gene and Total iron binding capacity function PMID 21483845 2011 An association between total iron binding capacity and SNP rs3811647 in the TF gene (GWAS observed P=7.0×10(-9), corrected P=0.012) was replicated within the VA samples (observed P=0.012).

rs3811647 in TF gene and Transferrin measurement PMID 25457201 2015 Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.

PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.