Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE We find that structure-based and PD-associated disease mutations in the WD40 domain including the common G2385R polymorphism mainly compromise dimer formation. 30635421

2019

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE LRRK2 p.G2385R is an Asian specific genetic risk factor for sporadic Parkinson's disease. 29414410

2018

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE Considering that there is overlap of the clinical manifestations and pathological characteristics between PD and MSA, we studied the possible associations between R1628P and G2385R polymorphisms of the LRRK2 and MSA in a population of Han Chinese patients. 25511328

2015

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China. 23624603

2013

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE LRRK2 Gly2385Arg polymorphism, cigarette smoking, and risk of sporadic Parkinson's disease: a case-control study in Japan. 20673920

2010

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population. 19854095

2010

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE The c.G4883C variant in the leucine-rich repeat kinase 2 (LRRK2) gene (protein effect: Arg1628Pro) has been recently proposed as a second risk factor for sporadic Parkinson's disease in the Han Chinese population (after the Gly2385Arg variant). 18716801

2008

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease. 17440812

2007

dbSNP: rs34778348
rs34778348
0.090 GeneticVariation BEFREE Our results suggest that the G2385R variant is a risk factor for sporadic Parkinson disease in the Asian population. 17314670

2007