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




[PMID 15759212] Identifying candidate Hirschsprung disease-associated RET variants.


[PMID 17267408] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.


[PMID 18091754] Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10.


[PMID 19138047] Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.


[PMID 20532249] Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.


[PMID 21349203] Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.


[PMID 10521317] Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.


[PMID 10922382] RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease.


[PMID 23059849] Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form


[PMID 24897126] RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease

rs1800858

Parent Gene: RET

Importance: 1
Less common allele: A = 25%
More common allele: G = 75%
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