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 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
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 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 There were no significant relationships between SNP rs356229, rs356219, or rs7684318 and the risk of sporadic PD in any genetic model. 22425546 2012