Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2736990
rs2736990
0.860 GeneticVariation BEFREE After narrowing down the variants using the <i>p</i> < 1 × 10<sup>-5</sup> cutoff, in overall populations, seven SNPs increased the risk of PD (rs2736990, rs356220, rs356165, rs181489, rs356219, rs11931074, and rs2737029, with odds ratios [ORs] of 1.22-1.38) and one SNP decreased the risk (rs356186, with an OR of 0.77). 30410434

2018

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation BEFREE Our meta-analysis provides evidence that the T allele, TT and TC genotype of rs2736990(C/T) polymorphism may decrease the risk of PD. 28844730

2017

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991

2014

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation BEFREE Our study demonstrated that SNCA rs2736990 C > T polymorphism was associated with susceptibility to PD in Chinese Han population. 24005725

2014

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation BEFREE Our results show that rs2736990 and rs356220 in SNCA decreased the risk for PD in a Chinese population. 25129240

2014

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation BEFREE In the additive model, SNP rs2736990 was significantly related to the risk of sporadic PD: the adjusted OR was 1.30 (95% CI: 1.002-1.68). 22425546

2012

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs2736990
rs2736990
0.860 GeneticVariation BEFREE Direct replication of SNPs within SNCA and BST1 confirmed these two genes to be associated with PD in the Netherlands (SNCA, rs2736990: P = 1.63 × 10(-5), OR = 1.325 and BST1, rs12502586: P = 1.63 × 10(-3), OR = 1.337). 21248740

2011

dbSNP: rs2736990
rs2736990
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
0.860 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010

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

2010

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

2009

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

2009