Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893829
rs104893829
VHL
T 0.810 CausalMutation CLINVAR

dbSNP: rs119103277
rs119103277
VHL
C 0.810 CausalMutation CLINVAR

dbSNP: rs119103277
rs119103277
VHL
A 0.810 CausalMutation CLINVAR

dbSNP: rs5030802
rs5030802
VHL
T 0.810 CausalMutation CLINVAR

dbSNP: rs5030804
rs5030804
VHL
T 0.810 CausalMutation CLINVAR

dbSNP: rs5030804
rs5030804
VHL
C 0.810 GeneticVariation CLINVAR

dbSNP: rs5030804
rs5030804
VHL
T 0.810 GeneticVariation CLINVAR

dbSNP: rs5030805
rs5030805
VHL
T 0.810 CausalMutation CLINVAR

dbSNP: rs5030821
rs5030821
VHL
C 0.810 GeneticVariation CLINVAR

dbSNP: rs587780077
rs587780077
VHL
A 0.810 CausalMutation CLINVAR

dbSNP: rs730882034
rs730882034
VHL
G 0.810 GeneticVariation CLINVAR

dbSNP: rs104893825
rs104893825
VHL
T 0.800 CausalMutation CLINVAR

dbSNP: rs104893830
rs104893830
VHL
C 0.800 CausalMutation CLINVAR

dbSNP: rs1352275281
rs1352275281
VHL
T 0.800 GeneticVariation CLINVAR

dbSNP: rs193922609
rs193922609
VHL
C 0.800 CausalMutation CLINVAR

dbSNP: rs193922609
rs193922609
VHL
A 0.800 GeneticVariation CLINVAR

dbSNP: rs193922609
rs193922609
VHL
C 0.800 GeneticVariation CLINVAR

dbSNP: rs397516444
rs397516444
VHL
A 0.800 CausalMutation CLINVAR

dbSNP: rs5030807
rs5030807
VHL
C 0.800 CausalMutation CLINVAR

dbSNP: rs5030808
rs5030808
VHL
C 0.800 GeneticVariation CLINVAR

dbSNP: rs5030808
rs5030808
VHL
T 0.800 CausalMutation CLINVAR

dbSNP: rs5030820
rs5030820
VHL
G 0.800 CausalMutation CLINVAR

dbSNP: rs5030822
rs5030822
VHL
A 0.800 CausalMutation CLINVAR

dbSNP: rs5030822
rs5030822
VHL
G 0.800 CausalMutation CLINVAR

dbSNP: rs5030826
rs5030826
VHL
A 0.800 CausalMutation CLINVAR