Disease: Parkinson Disease ×
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
0.810 GeneticVariation BEFREE Five out of the 13 tested SNPs (rs12185268, rs6599389, rs356220, rs13312, and rs17649553) were confirmed to be nominally significantly associated (<i>P</i> < 0.05) with PD risk in the Cypriot population. 31681140 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.810 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889 2014
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.810 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.810 GeneticVariation GWASCAT 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
0.810 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011