Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 GeneticVariation GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991

2014
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		G 0.900 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011