RS1781002042 UCHL1

Health Risk Chr 4:41257636
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Associated Conditions
Spastic paraplegia 79A
autosomal dominant
with ataxia
Spastic paraplegia 79A
autosomal dominant
with ataxia
Other Variants in UCHL1
rs1781001592 rs1310363710 rs2551922153 rs749368841 rs2154087189 rs2154087267 rs2154087252 rs2154087069 rs1781070341 rs121917767
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