Gene: VHL ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131690955
rs1131690955
VHL
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1131690956
rs1131690956
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131690958
rs1131690958
VHL
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1131690959
rs1131690959
VHL
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553619957
rs1553619957
VHL
T 0.700 CausalMutation CLINVAR

dbSNP: rs193922609
rs193922609
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs5030807
rs5030807
VHL
C 0.700 GeneticVariation CLINVAR

dbSNP: rs5030816
rs5030816
VHL
G 0.700 CausalMutation CLINVAR

dbSNP: rs5030824
rs5030824
VHL
G 0.700 CausalMutation CLINVAR

dbSNP: rs5030829
rs5030829
VHL
T 0.700 CausalMutation CLINVAR

dbSNP: rs730882030
rs730882030
VHL
A 0.700 CausalMutation CLINVAR

dbSNP: rs730882031
rs730882031
VHL
G 0.700 CausalMutation CLINVAR

dbSNP: rs730882037
rs730882037
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs730882039
rs730882039
VHL
A 0.700 CausalMutation CLINVAR

dbSNP: rs869025631
rs869025631
VHL
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131690964
rs1131690964
VHL
C 0.700 CausalMutation CLINVAR Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma. 7977367

1994
dbSNP: rs398123481
rs398123481
VHL
T 0.700 CausalMutation CLINVAR Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma. 7977367

1994
dbSNP: rs5030818
rs5030818
VHL
T 0.700 CausalMutation CLINVAR A novel mutation in the von Hippel-Lindau gene. 7987327

1994
dbSNP: rs5030820
rs5030820
VHL
T 0.700 CausalMutation CLINVAR Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. 7987306

1994
dbSNP: rs5030821
rs5030821
VHL
A 0.700 CausalMutation CLINVAR Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. 7987306

1994
dbSNP: rs5030821
rs5030821
VHL
C 0.700 CausalMutation CLINVAR Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. 7987306

1994
dbSNP: rs5030822
rs5030822
VHL
C 0.700 GeneticVariation CLINVAR Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. 7987306

1994
dbSNP: rs5030824
rs5030824
VHL
G 0.700 GeneticVariation CLINVAR Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. 7987306

1994
dbSNP: rs5030825
rs5030825
VHL
T 0.700 CausalMutation CLINVAR Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. 7987306

1994
dbSNP: rs5030830
rs5030830
VHL
C 0.700 CausalMutation CLINVAR Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. 7987306

1994