rs34637584, LRRK2

N. diseases: 78
Disease: Autosomal dominant late onset Parkinson disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autosomal dominant late onset Parkinson disease
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
0.010 GeneticVariation BEFREE Enhanced kinase activity of G2019S LRRK2 is a suspected mechanism for carriers to develop PD but pathophysiological function of G2019S LRRK2 is not clear. 25174649 2015