Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75030001
rs75030001
RET
T 0.700 CausalMutation CLINVAR Genotype-specific progression of hereditary medullary thyroid cancer. 29656518

2018

dbSNP: rs377767397
rs377767397
RET
A 0.700 CausalMutation CLINVAR Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families. 28099363

2017

dbSNP: rs377767397
rs377767397
RET
A 0.700 CausalMutation CLINVAR Distribution of RET Mutations in Multiple Endocrine Neoplasia 2 in Denmark 1994-2014: A Nationwide Study. 27809725

2017

dbSNP: rs75076352
rs75076352
RET
C 0.700 CausalMutation CLINVAR Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience. 28469506

2017

dbSNP: rs75996173
rs75996173
RET
A 0.700 CausalMutation CLINVAR Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience. 28469506

2017

dbSNP: rs146646971
rs146646971
RET
C 0.700 CausalMutation CLINVAR Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel. 26687385

2016

dbSNP: rs146646971
rs146646971
RET
T 0.700 CausalMutation CLINVAR Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation. 27673361

2016

dbSNP: rs146646971
rs146646971
RET
C 0.700 CausalMutation CLINVAR Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation. 27673361

2016

dbSNP: rs75076352
rs75076352
RET
C 0.700 CausalMutation CLINVAR Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. 27539324

2016

dbSNP: rs77939446
rs77939446
RET
A 0.700 CausalMutation CLINVAR Disease-modifying polymorphisms and C609Y mutation of RET associated with high penetrance of phaeochromocytoma and low rate of MTC in MEN2A. 27994876

2016

dbSNP: rs79658334
rs79658334
RET
A 0.700 CausalMutation CLINVAR How to Assess the Clinical Relevance of Novel RET Missense Variants in the Absence of Functional Studies? 27099842

2016

dbSNP: rs143795581
rs143795581
RET
G 0.700 CausalMutation CLINVAR Actionable exomic incidental findings in 6503 participants: challenges of variant classification. 25637381

2015

dbSNP: rs146646971
rs146646971
RET
T 0.700 CausalMutation CLINVAR Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients. 26269449

2015

dbSNP: rs146646971
rs146646971
RET
T 0.700 CausalMutation CLINVAR Actionable exomic incidental findings in 6503 participants: challenges of variant classification. 25637381

2015

dbSNP: rs146646971
rs146646971
RET
C 0.700 CausalMutation CLINVAR Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients. 26269449

2015

dbSNP: rs146646971
rs146646971
RET
C 0.700 CausalMutation CLINVAR Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. 25810047

2015

dbSNP: rs75030001
rs75030001
RET
T 0.700 CausalMutation CLINVAR Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. 25810047

2015

dbSNP: rs75076352
rs75076352
RET
C 0.700 CausalMutation CLINVAR RET Cys634Arg mutation confers a more aggressive multiple endocrine neoplasia type 2A phenotype than Cys634Tyr mutation. 25515555

2015

dbSNP: rs75996173
rs75996173
RET
A 0.700 CausalMutation CLINVAR Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. 25810047

2015

dbSNP: rs76262710
rs76262710
RET
A 0.700 CausalMutation CLINVAR Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. 25810047

2015

dbSNP: rs77316810
rs77316810
RET
G 0.700 CausalMutation CLINVAR Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma. 25694125

2015

dbSNP: rs79658334
rs79658334
RET
A 0.700 CausalMutation CLINVAR Characterization of V804M-mutated RET proto-oncogene associated with familial medullary thyroid cancer, report of the largest Turkish family. 25501606

2015

dbSNP: rs79658334
rs79658334
RET
A 0.700 CausalMutation CLINVAR Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma. 25810047

2015

dbSNP: rs79658334
rs79658334
RET
T 0.700 CausalMutation CLINVAR Actionable exomic incidental findings in 6503 participants: challenges of variant classification. 25637381

2015

dbSNP: rs79658334
rs79658334
RET
T 0.700 CausalMutation CLINVAR A NOVEL DOUBLE MUTATION VAL648ILE AND VAL804LEU OF RET PROTO-ONCOGENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2. 26247112

2015