RS869320761 VPS13C

Health Risk Chr 15:62013058
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive early-onset Parkinson disease 23
Autosomal recessive early-onset Parkinson disease 23
Other Variants in VPS13C
rs869312810 rs869312809 rs869312811 rs369100678 rs879253853 rs139665824 rs140338178 rs116803472 rs756128065 rs751295864
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