RS869312811 VPS13C

Health Risk Chr 15:61947292
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive early-onset Parkinson disease 23
Parkinson disease
Autosomal recessive early-onset Parkinson disease 23
Parkinson disease
Other Variants in VPS13C
rs869312810 rs869312809 rs369100678 rs879253853 rs869320761 rs139665824 rs140338178 rs116803472 rs756128065 rs751295864
Ask Dr. Hemsworth about this variant