Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR "Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 ""Janus"" genetic variation." 20152359 2010
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Actionable exomic incidental findings in 6503 participants: challenges of variant classification. 25637381 2015
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Predominant RET Germline Mutations in Exons 10, 11, and 16 in Iranian Patients with Hereditary Medullary Thyroid Carcinoma. 21765987 2011
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR RET revisited: expanding the oncogenic portfolio. 24561444 2014
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Patients with RET D631Y mutations most commonly present with pheochromocytoma and not medullary thyroid carcinoma. 22274720 2012
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma. 25319874 2014
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma. 22068382 2012
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern Chinese. 25628771 2015
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Patient affected by neurofibromatosis type 1 and thyroid C-cell hyperplasia harboring pathogenic germ-line mutations in both NF1 and RET genes. 24361808 2014
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Multiple endocrine neoplasia type 2: evaluation of the genotype-phenotype relationship. 12686527 2003
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden. 22270996 2012
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma. 25694125 2015
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR The clinical spectrum of RET proto-oncogene mutations in codon 790. 23756355 2013
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR The rare intracellular RET mutation p.S891A in a Chinese Han family with familial medullary thyroid carcinoma. 24845513 2014
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A. 9506724 1998
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation. 9384613 1998
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. 7907913 1994
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations. 12409662 2002
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significance. 9146685 1997
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family. 21678021 2011
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR How to Assess the Clinical Relevance of Novel RET Missense Variants in the Absence of Functional Studies? 27099842 2016
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Genotype-specific progression of hereditary medullary thyroid cancer. 29656518 2018
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Protecting thyroid cancer patients from untoward effects of radioactive iodine treatment. 19731974 2009
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease. 9067749 1997
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 CausalMutation group CLINVAR Impact of RET proto-oncogene analysis on the clinical management of multiple endocrine neoplasia type 2. 16532227 2006