rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
|
19574279 |
2009 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.
|
14500403 |
2003 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Germ-line mutations in nonsyndromic pheochromocytoma.
|
12000816 |
2002 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Systematic comparison of sporadic and syndromic pancreatic islet cell tumors.
|
20660572 |
2010 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma.
|
9829912 |
1998 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Genetic testing in pheochromocytoma or functional paraganglioma.
|
16314641 |
2005 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Local-regional recurrence of sporadic or syndromic abdominal extra-adrenal paraganglioma: incidence, characteristics, and outcome.
|
19958924 |
2009 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
|
19336503 |
2009 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions.
|
15300849 |
2004 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?
|
19029228 |
2009 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Calculating optimal surveillance for detection of von Hippel-Lindau-related manifestations.
|
24132471 |
2014 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Retinal hemangioblastoma in von Hippel-Lindau disease: a clinical and molecular study.
|
12202531 |
2002 |
rs397516441
|
Entrez Id: |
7428 |
Gene Symbol: |
VHL |
VHL
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
The Warburg effect is genetically determined in inherited pheochromocytomas.
|
19763184 |
2009 |