Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs33939927
rs33939927
LRRK2
0.030 GeneticVariation BEFREE Further analysis of family members of the proband with the p.R1441G mutation revealed that her mother and first cousin shared the same mutation and parkinsonism. 24973808

2014
dbSNP: rs33939927
rs33939927
LRRK2
0.030 GeneticVariation BEFREE Clinically, p.R1441C carriers had typical levodopa-responsive parkinsonism with tremor as the most common presenting feature. 18197194

2008
dbSNP: rs33939927
rs33939927
LRRK2
0.030 GeneticVariation BEFREE The distribution in age at onset and clinical features in Lrrk2 p.R1441C patients are similar to idiopathic and Lrrk2 p.G2019S parkinsonism. 18337586

2008