Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907571
rs387907571
DNAJC13
0.800 GeneticVariation UNIPROT

dbSNP: rs104886460
rs104886460
GBA
T 0.700 CausalMutation CLINVAR

dbSNP: rs1056737920
rs1056737920
TMEM230
0.700 GeneticVariation UNIPROT

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: rs193922928
rs193922928
ATXN3
CTGCTGCTGCTGCTGCTGCTGCTG 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs421016
rs421016
GBA
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs421016
rs421016
GBA
G 0.700 CausalMutation CLINVAR

dbSNP: rs63750424
rs63750424
MAPT
T 0.700 CausalMutation CLINVAR

dbSNP: rs63750756
rs63750756
MAPT
G 0.700 CausalMutation CLINVAR

dbSNP: rs63751273
rs63751273
MAPT
T 0.700 CausalMutation CLINVAR

dbSNP: rs63751392
rs63751392
MAPT
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs747427602
rs747427602
PRKN
0.700 GeneticVariation UNIPROT

dbSNP: rs75671029
rs75671029
GBA
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs75822236
rs75822236
GBA
T 0.700 CausalMutation CLINVAR

dbSNP: rs766013346
rs766013346
DNAJC13
0.700 GeneticVariation UNIPROT

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: rs9697983
rs9697983
GLUD2 ; LOC105373328
G 0.700 CausalMutation CLINVAR

dbSNP: rs894278
rs894278
SNCA
0.010 GeneticVariation BEFREE <b>Conclusions:</b> Hyposmia was associated with RBD in PD patients with the minor G allele of rs894278, which represent one specific subtype of PD. 28979204

2017