RS33939927 LRRK2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs33939927 represents a rare mutation in the LRRK2 gene on chromosome 12. The normal allele is (C)
Associated Conditions
Autosomal dominant Parkinson disease 8
Autosomal dominant Parkinson disease 8
Parkinson disease
late-onset
Autosomal dominant Parkinson disease 8
Autosomal dominant Parkinson disease 8
Autosomal dominant Parkinson disease 8
Parkinson disease
late-onset
Autosomal dominant Parkinson disease 8
Other Variants in LRRK2