LRRK2, leucine rich repeat kinase 2, 120892

N. diseases: 231; N. variants: 74
Disease: Autosomal Dominant Parkinsonism ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs33939927
rs33939927
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C0752098
Disease:
Autosomal Dominant Parkinsonism 		0.010 GeneticVariation BEFREE The Roc domain of the Lrrk2 protein harbors two pathogenic mutations which cause autosomal dominant parkinsonism (R1441C and R1441G). 18952485 2009