rs7684318, SNCA

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.730 GeneticVariation BEFREE There were no significant relationships between SNP rs356229, rs356219, or rs7684318 and the risk of sporadic PD in any genetic model. 22425546 2012
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.730 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.730 GeneticVariation BEFREE Our findings suggested that the SNP rs7684318 (T>C) transition of the SNCA gene contributes to PD susceptibility in Chinese Han population, which is consistent with the earlier study form Japan. 20513365 2010
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.730 GeneticVariation BEFREE In two independent case-control populations, we found that a SNP in alpha-synuclein (SNCA), r</span>s7684318, showed the strongest association with PD (P=5.0 x 10(-10)). 16500997 2006