TCF7L2

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 GeneRIF     6934
 dbSNP        6934
 PubMed     6934
 SADR     6934
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 HEFalMp     TCF7L2
Chromosome position Summary
Rs11196205 114797037114,797,037
Rs12255372 114798892114,798,892
Rs3814570 114698499114,698,499
Rs4506565 114746031114,746,031
Rs7901695 114744078114,744,078
Rs7903146 114748339114,748,339


These two snps rs12255372 and rs7903146 greatly influence your risk of Type-2 diabetes.

This has been confirmed by

  • several researchers ([PMID 16936217] [PMID 16855264] [1] [PMID 16936217])
  • Research [[2] [PMID 16936217] shows snps in the gene TCF7L2 significantly increases the risk of Type-2 diabetes.
  • Refining the impact of TCF7L2 gene variants on Type-2 diabetes and adaptive evolution [PMID 17206141].
  • [3] Carrying two copies of a common variant of TCF7L2 doubles your chances of developing Type-2 diabetes and puts you in a similar risk category to being clinically obese. A common variant of the gene increased the risk of developing diabetes by 50 per cent. Carrying two copies of the variant gene increased the risk two-fold, to nearly 100 per cent. In the population as a whole, the impact of this gene on the risk of developing diabetes is as big as the problem of being clinically obese (having a body mass index over 30).
  • Polymorphism in TCF7L2 is associated with reduced insulin secretion in nondiabetic women [PMID 17130514]


This news article summarizes how snps increase the risk



IHOP Information Hyperlinked Over Proteins.


PolyDoms Snap


[PMID 17519421] Variation in TCF7L2 influences therapeutic response to sulfonylureas - related to diabetes