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SNP information rs1799852

RS1799852

Normal allele: CC

A gene with a 40% effect on genetic variation in transferrin levels. Transferrin is the main iron transfer protein in plasma.

Polymorphism rs1799852 is related to topics like this:

Genetic haemochromatosis

Hereditary hemochromatosis is a genetic condition associated with severe liver disease and various...

Research and publications:

  16251468   Survey of allelic expression using EST mining.

  17601350   A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.

  19084217   Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

  19673882   A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.

  20095037   Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study.

  21978626   Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.

  22232660   Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene.

  22815867   Genetic determinants for body iron store and type 2 diabetes risk in US men and women.

  23386860   Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.

  23996192   Toenail iron, genetic determinants of iron status, and the risk of glioma.

  24391736   The contribution of diet and genotype to iron status in women: a classical twin study.

  26582562   Signatures of Evolutionary Adaptation in Quantitative Trait Loci Influencing Trace Element Homeostasis in Liver.

  27115882   Pre-treatment transferrin levels and genetic polymorphisms in the HFE gene as predictive markers of response to adalimumab in patients with Crohn's disease.

  27332551   Associations between Common Variants in Iron-Related Genes with Haematological Traits in Populations of African Ancestry.

  27437086   Allele Frequencies of the Single Nucleotide Polymorphisms Related to the Body Burden of Heavy Metals in the Korean Population and Their Ethnic Differences.

  33850216   Association of common TMPRSS6 and TF gene variants with hepcidin and iron status in healthy rural Gambians.

  34085096   Dietary iron to total energy intake ratio and type 2 diabetes incidence in a longitudinal 12-year analysis of the Korean Genome and Epidemiology Cohort Study.

  34790739   Association between serum iron status and primary liver cancer risk: a Mendelian randomization analysis.

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