Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5030826
rs5030826
VHL
T 0.800 CausalMutation CLINVAR

dbSNP: rs5030833
rs5030833
VHL
C 0.800 GeneticVariation CLINVAR

dbSNP: rs765978945
rs765978945
VHL
G 0.800 GeneticVariation CLINVAR

dbSNP: rs869025636
rs869025636
VHL
C 0.800 CausalMutation CLINVAR

dbSNP: rs869025660
rs869025660
VHL
T 0.800 CausalMutation CLINVAR

dbSNP: rs869025648
rs869025648
VHL
G 0.710 GeneticVariation CLINVAR

dbSNP: rs869025648
rs869025648
VHL
G 0.710 CausalMutation CLINVAR

dbSNP: rs869025667
rs869025667
VHL
C 0.710 GeneticVariation CLINVAR

dbSNP: rs1060503552
rs1060503552
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs1064796408
rs1064796408
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131690964
rs1131690964
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs143985153
rs143985153
VHL
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553619402
rs1553619402
VHL
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs1553619415
rs1553619415
VHL
CG 0.700 CausalMutation CLINVAR

dbSNP: rs1553619923
rs1553619923
VHL
TTAACAACCTTTGCTTGTCCCGATAGGTCACCTTTGGCTCTTCAGAGATGCAGGGA 0.700 GeneticVariation CLINVAR

dbSNP: rs1553619952
rs1553619952
VHL
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553619976
rs1553619976
VHL
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1553620331
rs1553620331
VHL
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1553620362
rs1553620362
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs1559425925
rs1559425925
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs1559425951
rs1559425951
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs1559426095
rs1559426095
VHL
C 0.700 CausalMutation CLINVAR

dbSNP: rs1559426115
rs1559426115
VHL
G 0.700 CausalMutation CLINVAR

dbSNP: rs1559426145
rs1559426145
VHL
GCC 0.700 CausalMutation CLINVAR

dbSNP: rs1559428051
rs1559428051
VHL
AC 0.700 CausalMutation CLINVAR