Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2736990
rs2736990
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.860 GeneticVariation GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991

2014
dbSNP: rs2736990
rs2736990
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.860 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs2736990
rs2736990
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.860 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011
dbSNP: rs2736990
rs2736990
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.860 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
dbSNP: rs2736990
rs2736990
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.860 GeneticVariation GWASDB Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
dbSNP: rs2736990
rs2736990
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		C 0.860 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009