Gene: SNCA ×
Source: GWASCAT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.900 GeneticVariation GWASCAT Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
G 0.900 GeneticVariation GWASCAT Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs11931074
rs11931074
SNCA ; LOC105377329
0.900 GeneticVariation GWASCAT Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. 19915576

2009
dbSNP: rs2736990
rs2736990
SNCA
0.860 GeneticVariation GWASCAT Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
dbSNP: rs2736990
rs2736990
SNCA
C 0.860 GeneticVariation GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASCAT SNCA_ rs356220 was associated with both Sporadic-PD (OR = 1.37, P = 1 × 10(-9)) and Familial-PD (OR = 1.40, P = 2 × 10(-5)). 24511991

2014
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
0.850 GeneticVariation GWASCAT Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
A 0.850 GeneticVariation GWASCAT Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. 21044948

2011
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation 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
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASCAT Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASCAT Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
dbSNP: rs356203
rs356203
SNCA
0.800 GeneticVariation GWASCAT Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms. 30957308

2019
dbSNP: rs356182
rs356182
SNCA ; LOC105377329
G 0.740 GeneticVariation GWASCAT A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. 28892059

2017
dbSNP: rs356182
rs356182
SNCA ; LOC105377329
0.740 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs356182
rs356182
SNCA ; LOC105377329
G 0.740 GeneticVariation GWASCAT Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. 25064009

2014
dbSNP: rs8180209
rs8180209
SNCA
0.700 GeneticVariation GWASCAT Genome-wide association study of Parkinson's disease in East Asians. 28011712

2017