RS33949390 LRRK2
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What This Variant Does
"Also known as R1628P, rs33949390 is a SNP in the LRRK2 gene. A study of Chinese patients with Parkin...
Associated Conditions
Autosomal dominant Parkinson disease 8
Early onset Alzheimer disease with behavioral disturbance
Spinocerebellar atrophy
Klippel-Feil syndrome 1
autosomal dominant
Parkinson disease
Autosomal dominant Parkinson disease 8
Autosomal dominant Parkinson disease 8
Early onset Alzheimer disease with behavioral disturbance
Spinocerebellar atrophy
Klippel-Feil syndrome 1
autosomal dominant
Parkinson disease
Autosomal dominant Parkinson disease 8
Other Variants in LRRK2