VHL, von Hippel-Lindau tumor suppressor, 7428

N. diseases: 372; N. variants: 215
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893829
rs104893829
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
T 0.810 CausalMutation CLINVAR
dbSNP: rs119103277
rs119103277
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
A 0.810 CausalMutation CLINVAR
dbSNP: rs119103277
rs119103277
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
C 0.810 CausalMutation CLINVAR
dbSNP: rs5030802
rs5030802
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
T 0.810 CausalMutation CLINVAR
dbSNP: rs5030804
rs5030804
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
C 0.810 GeneticVariation CLINVAR
dbSNP: rs5030804
rs5030804
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
T 0.810 GeneticVariation CLINVAR
dbSNP: rs5030804
rs5030804
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
T 0.810 CausalMutation CLINVAR
dbSNP: rs5030805
rs5030805
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
T 0.810 CausalMutation CLINVAR
dbSNP: rs5030821
rs5030821
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
C 0.810 GeneticVariation CLINVAR
dbSNP: rs5030824
rs5030824
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
0.810 GeneticVariation UNIPROT
dbSNP: rs5030824
rs5030824
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma
0.810 GeneticVariation UNIPROT
dbSNP: rs5030824
rs5030824
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma
G 0.810 CausalMutation CLINVAR
dbSNP: rs587780077
rs587780077
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
A 0.810 CausalMutation CLINVAR
dbSNP: rs730882034
rs730882034
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
G 0.810 GeneticVariation CLINVAR
dbSNP: rs104893825
rs104893825
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs104893826
rs104893826
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma
0.800 GeneticVariation UNIPROT
dbSNP: rs104893826
rs104893826
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma
C 0.800 CausalMutation CLINVAR
dbSNP: rs104893830
rs104893830
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs104893830
rs104893830
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C1837915
Disease:
ERYTHROCYTOSIS, FAMILIAL, 2
C 0.800 CausalMutation CLINVAR
dbSNP: rs104893831
rs104893831
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C1837915
Disease:
ERYTHROCYTOSIS, FAMILIAL, 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs1352275281
rs1352275281
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs193922609
rs193922609
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs193922609
rs193922609
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs193922609
rs193922609
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome
C 0.800 GeneticVariation CLINVAR
dbSNP: rs28940301
rs28940301
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C1837915
Disease:
ERYTHROCYTOSIS, FAMILIAL, 2
G 0.800 CausalMutation CLINVAR