RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Familial medullary thyroid carcinoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Three novel mutations in the RET proto-oncogene. 11692159 2001
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT A RET double mutation in the germline of a kindred with FMTC. 10826520 2000
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma. 10323403 1999
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma. 9677065 1998
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma. 9621513 1998
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A. 9506724 1998
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma. 9452077 1998
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma. 9398735 1997
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprinting. 9259198 1997
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTC. 9223675 1997
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations. 8807338 1996
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A. 8557249 1996
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC. 7845675 1995
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas. 8625130 1995
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT RET mutations in exons 13 and 14 of FMTC patients. 7784092 1995
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT RET proto-oncogene mutations in French MEN 2A and FMTC families. 7874109 1994
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene. 7881414 1994
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests. 7915165 1994
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer. 7849720 1994
dbSNP: rs55947360
rs55947360
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.700 GeneticVariation UNIPROT Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. 8103403 1993