Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9952724
rs9952724
CTIF
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs850084
rs850084
DPY19L2P3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs7846412
rs7846412
PIP4P2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs6757197
rs6757197
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs6460033
rs6460033
TYW1B
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs557074
rs557074
RREB1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs4746675
rs4746675
CTNNA3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs2862909
rs2862909
TPTE2P6 ; LOC105370117
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs2666781
rs2666781
DNAJC1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs213462
rs213462
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs1504212
rs1504212
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs1468375
rs1468375
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs13227860
rs13227860
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs12364577
rs12364577
LOC440040
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs12069733
rs12069733
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs10963676
rs10963676
ADAMTSL1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs10518765
rs10518765
UNC13C
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
dbSNP: rs11931074
rs11931074
SNCA ; LOC105377329
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs6812193
rs6812193
FAM47E ; FAM47E-STBD1 ; LOC105377286
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		T 0.880 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs2736990
rs2736990
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		C 0.860 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs823128
rs823128
NUCKS1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		C 0.850 GeneticVariation GWASDB We replicated the effect of a new locus detected in the Japanese cohort (PARK16, rs823128, OR = 0.66, P = 7.29 x 10(-8)) and provide supporting evidence that common variation around LRRK2 modulates risk for PD (rs1491923, OR = 1.14, P = 1.55 x 10(-5)). 19915575

2009
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		G 0.810 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs8070723
rs8070723
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs6532197
rs6532197
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		G 0.800 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs199533
rs199533
NSF ; LRRC37A2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		T 0.800 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009