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
0.740 GeneticVariation BEFREE In MR between α-synuclein in PD with AD risk, we only extracted rs356182 as the IV through a strict screening process. 30598082 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.740 GeneticVariation GWASCAT A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. 28892059 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.740 GeneticVariation BEFREE Common variant rs356182 near SNCA defines a Parkinson's disease endophenotype. 28078311 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.740 GeneticVariation BEFREE Here, in order to discover potential AD-related loci, we investigated the association between late-onset AD (LOAD) susceptibility and nine single-nucleotide polymorphisms (SNPs) (rs11724635 of BST1, rs12637471 of MCCC1, rs15553999 of TMEM229, rs17649553 of MAPT, rs34311866 of TMEM175-GAK-DGKQ, rs356182 of SNCA, rs6430538 of ACMSD-TMEM163, rs76904798 of LRRK2 and rs823118 of RAB7L1-NUCKS1) which were reported to have genome-wide significant associations with PD risk in a recent Genome Wide Association Study performed among white population. 26738859 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.740 GeneticVariation BEFREE Our study firstly demonstrates that SNCA rs356182 variant has an increased risk of susceptibility to PD in Han Chinese population. 27538639 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.740 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.740 GeneticVariation GWASCAT Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. 25064009 2014