rs143795581
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases.
|
15858153 |
2005 |
rs143795581
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Functional characterization of the MTC-associated germline RET-K666E mutation: evidence of oncogenic potential enhanced by the G691S polymorphism.
|
21690267 |
2011 |
rs143795581
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
|
25637381 |
2015 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro.
|
20103606 |
2010 |
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 |
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases.
|
15858153 |
2005 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma.
|
25319874 |
2014 |
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 |
Functional characterization of the MTC-associated germline RET-K666E mutation: evidence of oncogenic potential enhanced by the G691S polymorphism.
|
21690267 |
2011 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Predicting phenotypic severity of uncertain gene variants in the RET proto-oncogene.
|
21479187 |
2011 |
rs146646971
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases.
|
15858153 |
2005 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
|
25810047 |
2015 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family.
|
21678021 |
2011 |
rs146646971
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
|
27673361 |
2016 |
rs146646971
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro.
|
20103606 |
2010 |
rs377767397
|
|
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 |
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 |
rs377767397
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Unusual clinical presentation of a patient with multiple endocrine neoplasia type 2A.
|
11395220 |
2001 |
rs377767397
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutation screening in a Norwegian cohort with pheochromocytoma.
|
23407919 |
2013 |
rs377767397
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Sporadic versus familial medullary thyroid microcarcinoma: a histopathologic study of 50 consecutive patients.
|
11688458 |
2001 |
rs377767406
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A patient with MEN 2 and multiple mutations of RET in the germline.
|
11149622 |
2000 |