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SNP information rs17342717

RS17342717

Normal allele: CC

A common variant of the TFR2 gene involved in the physiological regulation of serum iron levels.

Polymorphism rs17342717 is related to topics like this:

Genetic haemochromatosis

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

Research and publications:

  20927387   A genome-wide association study of red blood cell traits using the electronic medical record.

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

  24270849   Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.

  26019233   Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

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

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

  31097152   Associations between single nucleotide polymorphisms and erythrocyte parameters in humans: A systematic literature review.

DNA test for autism

We recommend that anyone who has been diagnosed with autism undergo genetic testing. Unfortunately,...

Gene for lactose intolerance

Lactose intolerance is a condition characterized by difficulty digesting lactose, a sugar present...

CCNB1 cyclin B1

Cyclin B1 serves as a regulatory protein pivotal in the process of mitosis. It forms complexes with...

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