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A novel TCF7L2 type 2 diabetes SNP identified from fine mapping in African American women
SNP rs7903146 in the Wnt pathway’s TCF7L2 gene is the variant most significantly associated with type 2 diabetes to date, with associations observed across diverse populations. We sought to determine whether variants in other Wnt pathway genes are also associated with this disease. We evaluated 69 g...
Autores principales: | Haddad, Stephen A., Palmer, Julie R., Lunetta, Kathryn L., Ng, Maggie C. Y., Ruiz-Narváez, Edward A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333820/ https://www.ncbi.nlm.nih.gov/pubmed/28253288 http://dx.doi.org/10.1371/journal.pone.0172577 |
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