Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 162540
Gene Symbol: SPPL2C
SPPL2C
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: 54838
Gene Symbol: WBP1L
WBP1L
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: 119032
Gene Symbol: BORCS7
BORCS7
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: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB By comparing results of a GWAS performed on individuals of European ancestry, we identified PARK16, SNCA and LRRK2 as shared risk loci for PD and BST1 and MAPT as loci showing population differences. 19915576

2009
Entrez Id: 683
Gene Symbol: BST1
BST1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation GWASDB By comparing results of a GWAS performed on individuals of European ancestry, we identified PARK16, SNCA and LRRK2 as shared risk loci for PD and BST1 and MAPT as loci showing population differences. 19915576

2009
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. 19915576

2009
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
Entrez Id: 9842
Gene Symbol: PLEKHM1
PLEKHM1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
Entrez Id: 1620
Gene Symbol: BRINP1
BRINP1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
Entrez Id: 2580
Gene Symbol: GAK
GAK
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.480 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
Entrez Id: 4905
Gene Symbol: NSF
NSF
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.110 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
Entrez Id: 400952
Gene Symbol: LINC01121
LINC01121
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. 21044948

2011
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation GWASDB Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. 21044948

2011
Entrez Id: 147081
Gene Symbol: LINC02210
LINC02210
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. 21044948

2011
Entrez Id: 104909134
Gene Symbol: LINC02210-CRHR1
LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. 21044948

2011
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. 21084426

2011
Entrez Id: 2580
Gene Symbol: GAK
GAK
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation GWASDB Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study. 21258085

2011
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
Entrez Id: 683
Gene Symbol: BST1
BST1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.500 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
Entrez Id: 56922
Gene Symbol: MCCC1
MCCC1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.170 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
Entrez Id: 84660
Gene Symbol: CCDC62
CCDC62
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.170 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011