Normal allele: GG
Missense LRRK2 variant is a risk factor for Parkinson's disease.
Polymorphism rs7133914 is related to topics like this:
Research and publications:
18952485 Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
20186690 Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.
20301387 LRRK2 Parkinson Disease.
20669299 LRRK2 variation and Parkinson's disease in African Americans.
21885347 Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.
22373437 Identification of functional genetic variation in exome sequence analysis.