Gene: SNCA ×
Source: GWASDB ×
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 GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991 2014
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.700 GeneticVariation disease GWASDB Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204 2012
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.700 GeneticVariation disease GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.700 GeneticVariation disease GWASDB 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 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: 6622
Gene Symbol: SNCA
SNCA 		0.700 GeneticVariation disease 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 		0.700 GeneticVariation disease 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: 6622
Gene Symbol: SNCA
SNCA 		0.700 GeneticVariation disease 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 		0.700 GeneticVariation disease 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 		0.700 GeneticVariation disease 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: 6622
Gene Symbol: SNCA
SNCA 		0.700 GeneticVariation disease GWASDB Association to PD at SNCA was replicated in the Japanese GWAS, confirming this as a major risk locus across populations. 19915575 2009