Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878888
rs878888
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs878888
rs878888
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011