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: rs397516440
rs397516440
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.800 GeneticVariation CLINVAR
dbSNP: rs397516444
rs397516444
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		A 0.800 CausalMutation CLINVAR
dbSNP: rs5030807
rs5030807
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		C 0.800 CausalMutation CLINVAR
dbSNP: rs5030808
rs5030808
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		T 0.800 CausalMutation CLINVAR
dbSNP: rs5030808
rs5030808
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		C 0.800 GeneticVariation CLINVAR
dbSNP: rs5030808
rs5030808
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma 		A 0.800 CausalMutation CLINVAR
dbSNP: rs5030818
rs5030818
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		0.800 GeneticVariation UNIPROT
dbSNP: rs5030820
rs5030820
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma 		0.800 GeneticVariation UNIPROT
dbSNP: rs5030820
rs5030820
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma 		T 0.800 CausalMutation CLINVAR
dbSNP: rs5030820
rs5030820
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		G 0.800 CausalMutation CLINVAR
dbSNP: rs5030822
rs5030822
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		A 0.800 CausalMutation CLINVAR
dbSNP: rs5030822
rs5030822
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		G 0.800 CausalMutation CLINVAR
dbSNP: rs5030824
rs5030824
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C1837915
Disease:
ERYTHROCYTOSIS, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT
dbSNP: rs5030826
rs5030826
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		A 0.800 CausalMutation CLINVAR
dbSNP: rs5030826
rs5030826
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		T 0.800 CausalMutation CLINVAR
dbSNP: rs5030833
rs5030833
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		C 0.800 GeneticVariation CLINVAR
dbSNP: rs765978945
rs765978945
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		G 0.800 GeneticVariation CLINVAR
dbSNP: rs869025636
rs869025636
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		C 0.800 CausalMutation CLINVAR
dbSNP: rs869025660
rs869025660
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		T 0.800 CausalMutation CLINVAR
dbSNP: rs5030805
rs5030805
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma 		0.710 GeneticVariation UNIPROT
dbSNP: rs5030809
rs5030809
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0031511
Disease:
Pheochromocytoma 		0.710 GeneticVariation UNIPROT
dbSNP: rs5030812
rs5030812
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		0.710 GeneticVariation UNIPROT
dbSNP: rs869025648
rs869025648
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		G 0.710 CausalMutation CLINVAR
dbSNP: rs869025648
rs869025648
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		G 0.710 GeneticVariation CLINVAR
dbSNP: rs869025667
rs869025667
Entrez Id: 7428
Gene Symbol: VHL
VHL
CUI: C0019562
Disease:
Von Hippel-Lindau Syndrome 		C 0.710 GeneticVariation CLINVAR