Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4746675
rs4746675
CTNNA3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006