Gene: RET ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360

2017
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175

2015
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965

2015
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249

2013
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT Clinical utility gene card for: multiple endocrine neoplasia type 2. 21863057

2012
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT Medullary thyroid cancer: management guidelines of the American Thyroid Association. 19469690

2009
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT Guidelines for diagnosis and therapy of MEN type 1 and type 2. 11739416

2001
dbSNP: rs79658334
rs79658334
RET
0.880 GeneticVariation UNIPROT 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: rs79658334
rs79658334
RET
T 0.880 CausalMutation CLINVAR

dbSNP: rs79658334
rs79658334
RET
A 0.880 CausalMutation CLINVAR

dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360

2017
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965

2015
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175

2015
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249

2013
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT Clinical utility gene card for: multiple endocrine neoplasia type 2. 21863057

2012
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT Medullary thyroid cancer: management guidelines of the American Thyroid Association. 19469690

2009
dbSNP: rs75234356
rs75234356
RET
0.870 GeneticVariation UNIPROT Three novel mutations in the RET proto-oncogene. 11692159

2001
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT Three novel mutations in the RET proto-oncogene. 11692159

2001
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT Guidelines for diagnosis and therapy of MEN type 1 and type 2. 11739416

2001
dbSNP: rs75234356
rs75234356
RET
0.870 GeneticVariation UNIPROT A RET double mutation in the germline of a kindred with FMTC. 10826520

2000
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT A RET double mutation in the germline of a kindred with FMTC. 10826520

2000
dbSNP: rs75234356
rs75234356
RET
0.870 GeneticVariation UNIPROT A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma. 10323403

1999
dbSNP: rs76262710
rs76262710
RET
0.870 GeneticVariation UNIPROT A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma. 10323403

1999
dbSNP: rs75234356
rs75234356
RET
0.870 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: rs75234356
rs75234356
RET
0.870 GeneticVariation UNIPROT Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma. 9621513

1998