RS11564176 LRRK2

Health Risk Chr 12:40322036 snv stop gained
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Associated Conditions
Autosomal dominant Parkinson disease 8
Autosomal dominant Parkinson disease 8
Population Frequencies
gnomAD ALL
0%
Other Variants in LRRK2
rs33939927 rs35801418 rs34805604 rs34637584 rs35870237 rs34995376 rs34778348 rs78501232 rs35328937 rs7308720
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