Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.700 GeneticVariation disease GWASCAT 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: 6622
Gene Symbol: SNCA
SNCA
0.700 GeneticVariation disease GWASCAT Association to PD at SNCA was replicated in the Japanese GWAS, confirming this as a major risk locus across populations. 19915575 2009
Entrez Id: 2580
Gene Symbol: GAK
GAK
0.500 GeneticVariation disease GWASCAT Genomewide association study for susceptibility genes contributing to familial Parkinson disease. 18985386 2009
Entrez Id: 683
Gene Symbol: BST1
BST1
0.500 GeneticVariation disease GWASCAT 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: 64710
Gene Symbol: NUCKS1
NUCKS1
0.130 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 100631383
Gene Symbol: FAM47E-STBD1
FAM47E-STBD1
0.110 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 4905
Gene Symbol: NSF
NSF
0.110 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 100129583
Gene Symbol: FAM47E
FAM47E
0.110 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 104909134
Gene Symbol: LINC02210-CRHR1
LINC02210-CRHR1
0.100 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 147081
Gene Symbol: LINC02210
LINC02210
0.100 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 54838
Gene Symbol: WBP1L
WBP1L
0.100 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 1586
Gene Symbol: CYP17A1
CYP17A1
0.100 GeneticVariation disease GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
0.100 GeneticVariation disease GWASCAT 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
0.700 GeneticVariation disease GWASCAT 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
0.700 GeneticVariation disease GWASCAT Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850 2010
Entrez Id: 2580
Gene Symbol: GAK
GAK
0.500 GeneticVariation disease GWASCAT 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
0.480 GeneticVariation disease GWASCAT 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
0.110 GeneticVariation disease GWASCAT Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177 2010
Entrez Id: 9842
Gene Symbol: PLEKHM1
PLEKHM1
0.100 GeneticVariation disease GWASCAT 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
0.100 GeneticVariation disease GWASCAT 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
0.700 GeneticVariation disease GWASCAT Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.700 GeneticVariation disease GWASCAT 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
0.700 GeneticVariation disease GWASCAT 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: 6622
Gene Symbol: SNCA
SNCA
0.700 GeneticVariation disease GWASCAT 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: 120892
Gene Symbol: LRRK2
LRRK2
0.500 GeneticVariation disease GWASCAT Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011