rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
27854360
2017
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
24893135
2014
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Canadian guideline on genetic screening for hereditary renal cell cancers.
24319509
2013
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
CLINVAR
Systematic comparison of sporadic and syndromic pancreatic islet cell tumors.
20660572
2010
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
GeneticVariation
CLINVAR
Genetic analysis of von Hippel-Lindau disease.
20151405
2010
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
CLINVAR
Genetic analysis of von Hippel-Lindau disease.
20151405
2010
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
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
Von Hippel-Lindau Syndrome
G
0.800
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
Von Hippel-Lindau Syndrome
G
0.800
GeneticVariation
CLINVAR
The Warburg effect is genetically determined in inherited pheochromocytomas.
19763184
2009
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
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
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
CLINVAR
The Warburg effect is genetically determined in inherited pheochromocytomas.
19763184
2009
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
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
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
CLINVAR
Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?
19029228
2009
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
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
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
The von Hippel-Lindau (VHL) germline mutation V84L manifests as early-onset bilateral pheochromocytoma.
16502427
2006
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
GeneticVariation
CLINVAR
Genetic testing in pheochromocytoma or functional paraganglioma.
16314641
2005
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
CLINVAR
Genetic testing in pheochromocytoma or functional paraganglioma.
16314641
2005
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.
15604628
2004
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
CLINVAR
Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions.
15300849
2004
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
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
Von Hippel-Lindau Syndrome
G
0.800
CausalMutation
CLINVAR
Hereditary phaeochromocytomas and paragangliomas: a study of five susceptibility genes.
12807974
2003
rs397516441
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.800
GeneticVariation
CLINVAR
Germ-line mutations in nonsyndromic pheochromocytoma.
12000816
2002