Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson 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
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		G 0.810 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009