rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genotype-specific progression of hereditary medullary thyroid cancer.
|
29656518 |
2018 |
rs377767397
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families.
|
28099363 |
2017 |
rs377767397
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Distribution of RET Mutations in Multiple Endocrine Neoplasia 2 in Denmark 1994-2014: A Nationwide Study.
|
27809725 |
2017 |
rs75076352
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience.
|
28469506 |
2017 |
rs75996173
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience.
|
28469506 |
2017 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
|
26687385 |
2016 |
rs146646971
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
|
27673361 |
2016 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
|
27673361 |
2016 |
rs75076352
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
|
27539324 |
2016 |
rs77939446
|
|
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 |
rs79658334
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
How to Assess the Clinical Relevance of Novel RET Missense Variants in the Absence of Functional Studies?
|
27099842 |
2016 |
rs143795581
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
|
25637381 |
2015 |
rs146646971
|
|
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 |
rs146646971
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
|
25637381 |
2015 |
rs146646971
|
|
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 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
|
25810047 |
2015 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
|
25810047 |
2015 |
rs75076352
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
RET Cys634Arg mutation confers a more aggressive multiple endocrine neoplasia type 2A phenotype than Cys634Tyr mutation.
|
25515555 |
2015 |
rs75996173
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
|
25810047 |
2015 |
rs76262710
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
|
25810047 |
2015 |
rs77316810
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma.
|
25694125 |
2015 |
rs79658334
|
|
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 |
rs79658334
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
|
25810047 |
2015 |
rs79658334
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
|
25637381 |
2015 |
rs79658334
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A NOVEL DOUBLE MUTATION VAL648ILE AND VAL804LEU OF RET PROTO-ONCOGENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2.
|
26247112 |
2015 |