Normal allele: CC
A break in the LRRK2 gene is associated with essential tremor and Parkinson's disease.
Polymorphism rs34594498 is related to topics like this:
Research and publications:
20301387 LRRK2 Parkinson Disease.
21885347 Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.
26234753 The LRRK2 A419V variant is a risk factor for Parkinson's disease in the Asian population.
27653456 Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease.
29812962 Genetic Analysis of LRRK1 and LRRK2 Variants in Essential Tremor Patients.