Gene: RET ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79658334
rs79658334
RET
A 0.700 GeneticVariation CLINVAR

dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects. 7608256

1995
dbSNP: rs79658334
rs79658334
RET
T 0.700 CausalMutation CLINVAR RET mutations in exons 13 and 14 of FMTC patients. 7784092

1995
dbSNP: rs75076352
rs75076352
RET
C 0.700 CausalMutation CLINVAR Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B. 7824936

1995
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer. 7849720

1994
dbSNP: rs77939446
rs77939446
RET
A 0.700 CausalMutation CLINVAR RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer. 7849720

1994
dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR RET proto-oncogene mutations in French MEN 2A and FMTC families. 7874109

1994
dbSNP: rs77316810
rs77316810
RET
C 0.700 CausalMutation CLINVAR RET proto-oncogene mutations in French MEN 2A and FMTC families. 7874109

1994
dbSNP: rs75996173
rs75996173
RET
A 0.700 CausalMutation CLINVAR Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene. 7881414

1994
dbSNP: rs75076352
rs75076352
RET
C 0.700 CausalMutation CLINVAR Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. 7907913

1994
dbSNP: rs377767397
rs377767397
RET
A 0.700 CausalMutation CLINVAR 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: rs79781594
rs79781594
RET
T 0.700 CausalMutation CLINVAR 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: rs75076352
rs75076352
RET
C 0.700 CausalMutation CLINVAR The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. 8918855

1996
dbSNP: rs77316810
rs77316810
RET
G 0.700 CausalMutation CLINVAR The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. 8918855

1996
dbSNP: rs79781594
rs79781594
RET
A 0.700 CausalMutation CLINVAR The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. 8918855

1996
dbSNP: rs75996173
rs75996173
RET
A 0.700 CausalMutation CLINVAR Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease. 9067749

1997
dbSNP: rs77316810
rs77316810
RET
G 0.700 CausalMutation CLINVAR Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease. 9067749

1997
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma. 9068588

1997
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significance. 9146685

1997
dbSNP: rs79781594
rs79781594
RET
T 0.700 CausalMutation CLINVAR RET in human development and oncogenesis. 9174404

1997
dbSNP: rs79658334
rs79658334
RET
T 0.700 CausalMutation CLINVAR Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain. 9242375

1997
dbSNP: rs77939446
rs77939446
RET
A 0.700 CausalMutation CLINVAR Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation. 9384613

1998
dbSNP: rs79890926
rs79890926
RET
G 0.700 CausalMutation CLINVAR Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation. 9384613

1998
dbSNP: rs79658334
rs79658334
RET
T 0.700 CausalMutation CLINVAR A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma. 9398735

1997
dbSNP: rs79658334
rs79658334
RET
T 0.700 CausalMutation CLINVAR 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