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SNP information rs1800860

RS1800860

Normal allele: AA

RET tagSNP polymorphism is associated with clinical severity and thyroid function in patients with differentiated thyroid cancer.

Polymorphism rs1800860 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:

  12872262   Novel intronic polymorphisms in the RET proto-oncogene and their association with Hirschsprung disease.

  16424056   Polymorphisms in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A.

  18820179   A common RET variant is associated with reduced newborn kidney size and function.

  20454948   Association analysis of the RET proto-oncogene with Hirschsprung disease in the Han Chinese population of southeastern China.

  20532249   Haplotype analysis revealed a possible founder effect of the RET R114H mutation in Hirschsprung disease in a Chinese population.

  21349203   RET genetic variants and risk of Hirschsprung's disease in Southeast China: a haplotype-based analysis.

  21821672   A variant OSR1 allele which disturbs OSR1 mRNA expression in renal progenitor cells is associated with reduction of newborn kidney size and function.

  22035350   Evaluation of High Resolution Melting analysis as an alternate tool to screen for risk alleles associated with small kidneys in Indian newborns.

  23084198   Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations.

  23757202   Free the data: one laboratory's approach to knowledge-based classification of genomic variants and preparation for integration of genomic data into EMR.

  24897126   RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.

  25310821   A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.

  25741868   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

  27533506   Association Between RET (rs1800860) and GFRA1 (rs45568534, rs8192663, rs181595401, rs7090693, and rs2694770) Variants and Kidney Size in Healthy Newborns.

  29131865   Associations between RET tagSNPs and their haplotypes and susceptibility, clinical severity, and thyroid function in patients with differentiated thyroid cancer.

  33342844   Study of genetic polymorphism of the RET proto-oncogene in Hirschsprung's disease in children.

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