Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730882034
rs730882034
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		G 0.810 GeneticVariation CLINVAR

dbSNP: rs587780077
rs587780077
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		A 0.810 CausalMutation CLINVAR

dbSNP: rs5030821
rs5030821
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.810 GeneticVariation CLINVAR

dbSNP: rs5030805
rs5030805
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.810 CausalMutation CLINVAR

dbSNP: rs5030804
rs5030804
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.810 GeneticVariation CLINVAR

dbSNP: rs5030804
rs5030804
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.810 GeneticVariation CLINVAR

dbSNP: rs5030804
rs5030804
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.810 CausalMutation CLINVAR

dbSNP: rs5030802
rs5030802
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.810 CausalMutation CLINVAR

dbSNP: rs119103277
rs119103277
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		A 0.810 CausalMutation CLINVAR

dbSNP: rs119103277
rs119103277
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.810 CausalMutation CLINVAR

dbSNP: rs104893829
rs104893829
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.810 CausalMutation CLINVAR

dbSNP: rs869025660
rs869025660
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.800 CausalMutation CLINVAR

dbSNP: rs869025636
rs869025636
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.800 CausalMutation CLINVAR

dbSNP: rs765978945
rs765978945
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		G 0.800 GeneticVariation CLINVAR

dbSNP: rs5030833
rs5030833
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.800 GeneticVariation CLINVAR

dbSNP: rs5030826
rs5030826
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.800 CausalMutation CLINVAR

dbSNP: rs5030826
rs5030826
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs5030822
rs5030822
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs5030822
rs5030822
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		G 0.800 CausalMutation CLINVAR

dbSNP: rs5030820
rs5030820
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		G 0.800 CausalMutation CLINVAR

dbSNP: rs5030808
rs5030808
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.800 GeneticVariation CLINVAR

dbSNP: rs5030808
rs5030808
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		T 0.800 CausalMutation CLINVAR

dbSNP: rs5030807
rs5030807
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.800 CausalMutation CLINVAR

dbSNP: rs397516444
rs397516444
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs193922609
rs193922609
VHL
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		C 0.800 CausalMutation CLINVAR