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SNP information rs2439302

Normal allele: CC

The rs2439302 polymorphism is associated with thyroid cancer.

Polymorphism rs2439302 is related to topics like this:

Genetic testing for thyroid cancer

Thyroid cancer is a prevalent type of malignancy in the endocrine system. Children who undergo...

Research and publications:

  22267200   Discovery of common variants associated with low TSH levels and thyroid cancer risk.

  23408906   A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.

  23847140   Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population.

  24144365   Familial multinodular goiter syndrome with papillary thyroid carcinomas: mutational analysis of the associated genes in 5 cases from 1 Chinese family.

  24591304   Significant SNPs have limited prediction ability for thyroid cancer.

  25562676   The common genetic variant rs944289 on chromosome 14q13.3 associates with risk of both malignant and benign thyroid tumors in the Japanese population.

  25743335   Whole-genome sequence-based analysis of thyroid function.

  26490305   Association between GWAS-Derived rs966423 Genetic Variant and Overall Mortality in Patients with Differentiated Thyroid Cancer.

  27079684   Genome-wide association studies and epigenome-wide association studies go together in cancer control.

  27342578   Papillary Thyroid Carcinoma: Association Between Germline DNA Variant Markers and Clinical Parameters.

  27512836   Clinical features of Hispanic thyroid cancer cases and the role of known genetic variants on disease risk.

  28256518   Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

  28499365   Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

  29121253   The Role of NRG1 in the Predisposition to Papillary Thyroid Carcinoma.

  30089490   Thyroid cancers of follicular origin in a genomic light: in-depth overview of common and unique molecular marker candidates.

  31738640   Association of neuregulin 1 polymorphisms rs7835688-Gâu003e-C, rs16879552 T-u003e-C and rs2439302-G-u003e-C with susceptibility to non-syndromic Hirschsprung disease.

  33551988   The Contribution of Genetic Variants to the Risk of Papillary Thyroid Carcinoma in the Kazakh Population: Study of Common Single Nucleotide Polymorphisms and Their Clinicopathological Correlations.

  34950210   Genetic Variants Associated with Thyroid Cancer Risk: Comprehensive Research Synopsis, Meta-Analysis, and Cumulative Epidemiological Evidence.

  35558387   Investigating the Association Between rs2439302 Polymorphism and Thyroid Cancer: A Systematic Review and Meta-Analysis.

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