rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Preventive medicine of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumors.
29748190
2018
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB , and SDHD Genes: Thai Experience.
28469506
2017
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients.
22357542
2012
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
VHL gene mutations and their effects on hypoxia inducible factor HIFα: identification of potential driver and passenger mutations.
21715564
2011
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Genetic analysis of von Hippel-Lindau disease.
20151405
2010
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes.
20054297
2010
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Structural bioinformatics mutation analysis reveals genotype-phenotype correlations in von Hippel-Lindau disease and suggests molecular mechanisms of tumorigenesis.
19408298
2009
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Improved identification of von Hippel-Lindau gene alterations in clear cell renal tumors.
18676741
2008
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Genotype-phenotype correlations in von Hippel-Lindau disease.
17024664
2007
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.
17661816
2007
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
Neutrophils from patients with heterozygous germline mutations in the von Hippel Lindau protein (pVHL) display delayed apoptosis and enhanced bacterial phagocytosis.
16809612
2006
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
C
0.700
CausalMutation
CLINVAR
The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system.
10567493
1999
rs869025655
×
Entrez Id:
7428
Gene Symbol:
VHL
VHL
Von Hippel-Lindau Syndrome
G
0.700
CausalMutation
CLINVAR