rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
RET proto-oncogene genetic screening of families with multiple endocrine neoplasia type 2 optimizes diagnostic and clinical management in China.
|
23210566 |
2012 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Hereditary medullary thyroid cancer in Slovenia--genotype-phenotype correlations.
|
16865646 |
2006 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
|
25810047 |
2015 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations.
|
12409662 |
2002 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Role of prophylactic thyroidectomy in RET 790 familial medullary thyroid carcinoma.
|
21688339 |
2012 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center.
|
17895320 |
2007 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Failure of pentagastrin-stimulated calcitonin testing in early manifestation of familial medullary thyroid cancer.
|
22965292 |
2012 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Papillary thyroid carcinoma in patients with RET proto-oncogene germline mutation.
|
12193298 |
2002 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A.
|
9506724 |
1998 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Medullary thyroid cancer: management guidelines of the American Thyroid Association.
|
19469690 |
2009 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The clinical spectrum of RET proto-oncogene mutations in codon 790.
|
23756355 |
2013 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Bilateral adrenal pheochromocytoma with a germline L790F mutation in the RET oncogene.
|
22403753 |
2012 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genotype-specific progression of hereditary medullary thyroid cancer.
|
29656518 |
2018 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
In silico and in vitro analysis of rare germline allelic variants of RET oncogene associated with medullary thyroid cancer.
|
21810974 |
2011 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
RET proto-oncogene mutations affecting codon 790/791: A mild form of multiple endocrine neoplasia type 2A syndrome?
|
12490841 |
2002 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Familial prevalence and age of RET germline mutations: implications for screening.
|
18062802 |
2008 |