RS35870237 LRRK2

Health Risk Chr 12:40340404
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What This Variant Does
"c.6059T&gt
Associated Conditions
Autosomal dominant Parkinson disease 8
Autosomal dominant Parkinson disease 8
Other Variants in LRRK2
rs33939927 rs35801418 rs34805604 rs34637584 rs34995376 rs34778348 rs78501232 rs35328937 rs7308720 rs35173587
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