Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104886460
rs104886460
GBA
T 0.700 CausalMutation CLINVAR

dbSNP: rs1064651
rs1064651
GBA
G 0.700 CausalMutation CLINVAR

dbSNP: rs1237637353
rs1237637353
GBA
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557901552
rs1557901552
GBA
T 0.700 CausalMutation CLINVAR

dbSNP: rs421016
rs421016
GBA
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs421016
rs421016
GBA
G 0.700 CausalMutation CLINVAR

dbSNP: rs75671029
rs75671029
GBA
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs75822236
rs75822236
GBA
T 0.700 CausalMutation CLINVAR

dbSNP: rs76763715
rs76763715
GBA
C 0.700 CausalMutation CLINVAR

dbSNP: rs76763715
rs76763715
GBA
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs78973108
rs78973108
GBA
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356769
rs80356769
GBA
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356771
rs80356771
GBA
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356771
rs80356771
GBA
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs1450426641
rs1450426641
GBA
0.010 GeneticVariation BEFREE A GBA p.Trp378Gly mutation was identified in two RBD and four PD patients (1% of all patients combined), and not in controls. 29920646

2018

dbSNP: rs2230288
rs2230288
GBA
0.010 GeneticVariation BEFREE The discovery that E326K</span> negatively impacts cognitive performance approximately doubles the proportion of PD patients we now recognize are at risk for more severe GBA-related cognitive deficits. 26296077

2016