ClinVar Miner

List of variants in gene UCHL1 reported as benign for Parkinson disease

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_004181.4(UCHL1):c.-71C>G rs201100258
NM_004181.5(UCHL1):c.*294G>A rs116700032
NM_004181.5(UCHL1):c.*309T>C rs78683791
NM_004181.5(UCHL1):c.-16C>T rs9321
NM_004181.5(UCHL1):c.-24A>G rs11556271
NM_004181.5(UCHL1):c.45+6T>C rs11556273
NM_004181.5(UCHL1):c.53C>A (p.Ser18Tyr) rs5030732
NM_004181.5(UCHL1):c.558C>T (p.Gly186=) rs116680633
NM_004181.5(UCHL1):c.609A>G (p.Glu203=) rs147661219

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