RS121917767 UCHL1

Health Risk Chr 4:41260751
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Parkinson disease 5
autosomal dominant
susceptibility to
Parkinson disease 5
autosomal dominant
susceptibility to
Other Variants in UCHL1
rs1781070341 rs1310363710 rs2551922153 rs1781002042 rs749368841 rs2154087189 rs2154087267 rs2154087252 rs2154087069 rs397515634
Ask Dr. Hemsworth about this variant