Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6239
Gene Symbol: RREB1
RREB1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.110 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 441250
Gene Symbol: TYW1B
TYW1B
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 64215
Gene Symbol: DNAJC1
DNAJC1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 92949
Gene Symbol: ADAMTSL1
ADAMTSL1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 440279
Gene Symbol: UNC13C
UNC13C
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 442524
Gene Symbol: DPY19L2P3
DPY19L2P3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 374491
Gene Symbol: TPTE2P6
TPTE2P6
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 29119
Gene Symbol: CTNNA3
CTNNA3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 55529
Gene Symbol: PIP4P2
PIP4P2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006

Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Association to PD at SNCA was replicated in the Japanese GWAS, confirming this as a major risk locus across populations. 19915575

2009

Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.500 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 64710
Gene Symbol: NUCKS1
NUCKS1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.130 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 100128977
Gene Symbol: MAPT-AS1
MAPT-AS1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.120 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 100631383
Gene Symbol: FAM47E-STBD1
FAM47E-STBD1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.110 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 100129583
Gene Symbol: FAM47E
FAM47E
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.110 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 284058
Gene Symbol: KANSL1
KANSL1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.110 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 4905
Gene Symbol: NSF
NSF
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.110 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 147081
Gene Symbol: LINC02210
LINC02210
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 54805
Gene Symbol: CNNM2
CNNM2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 104909134
Gene Symbol: LINC02210-CRHR1
LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 1586
Gene Symbol: CYP17A1
CYP17A1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 9842
Gene Symbol: PLEKHM1
PLEKHM1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 148811
Gene Symbol: PM20D1
PM20D1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

Entrez Id: 100528007
Gene Symbol: BORCS7-ASMT
BORCS7-ASMT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009