Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs33939927
rs33939927
LRRK2
0.020 GeneticVariation BEFREE All six p.R1441C carriers were familial PD patients explaining 10.7% of familial PD in the Belgian patient group. 18197194

2008
dbSNP: rs33939927
rs33939927
LRRK2
0.020 GeneticVariation BEFREE We show that LRRK2 immunoprecipitated from cells has a detectable GTPase activity that is disrupted by a familial mutation associated with PD located within the GTPase domain, R1441C. 17442267

2007