Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1442190
rs1442190
CNTN1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889

2014