|?|| (C;C) (C;G) (G;G) ||28|
|| [PMID 22267200]
|| Discovery of common variants associated with low TSH levels and thyroid cancer risk.
| Risk Allele
| Odds Ratio
|| 1.3600 None
[PMID 23659773] Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma
[PMID 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
[PMID 24591304] Significant SNPs have limited prediction ability for thyroid cancer
[PMID 25746573] Clinical significance of papillary thyroid cancer risk loci identified by genome-wide association studies
[PMID 26490305] Association Between GWAS-derived rs966423 Genetic Variant and Overall Mortality in Patients with Differentiated Thyroid Cancer
[PMID 28256518] Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.