rs1553620313
×
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
rs1553620313
×
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
rs1553620313
×
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
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.800
CausalMutation
CLINVAR
VHL and HIF-1α: gene variations and prognosis in early-stage clear cell renal cell carcinoma.
24446253
2014
rs1553620313
×
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
rs1553620313
×
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
rs1553620313
×
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
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.800
CausalMutation
CLINVAR
Improved detection of germline mutations in Korean VHL patients by multiple ligation-dependent probe amplification analysis.
19270817
2009
rs1553620313
×
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
rs1553620313
×
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
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.800
CausalMutation
CLINVAR
VHL gene alterations in renal cell carcinoma patients: novel hotspot or founder mutations and linkage disequilibrium.
11536052
2001
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.800
CausalMutation
CLINVAR
Germ-line mutation analysis in patients with von Hippel-Lindau disease in Japan: an extended study of 77 families.
10761708
2000
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Formation of the VHL-elongin BC tumor suppressor complex is mediated by the chaperonin TRiC.
10635329
1999
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC.
10408776
1999
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene.
10533030
1999
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Variable penetrance of familial pheochromocytoma associated with the von Hipple Lindau gene mutation, S68W. Mutations in brief no. 150. Online.
10627136
1998
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma.
9829912
1998
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene.
9829911
1998
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Germline mutations detected in the von Hippel-Lindau disease tumor suppressor gene by Southern blot and direct genomic DNA sequencing.
9452032
1998
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Three novel mutations in the Von Hippel-Lindau tumour suppressor gene in Italian patients.
9452106
1998
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.800
CausalMutation
CLINVAR
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
8956040
1996
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.
8730290
1996
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
8956040
1996
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.800
CausalMutation
CLINVAR
Molecular genetic diagnosis of von Hippel-Lindau disease: analysis of five Japanese families.
8641976
1996
rs1553620313
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
0.800
GeneticVariation
UNIPROT
Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.
8592333
1995