List of variants in gene UCHL1 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_004181.5(UCHL1):c.53C>A (p.Ser18Tyr)	rs5030732	0.16658
NM_004181.5(UCHL1):c.-24A>G	rs11556271	0.11322
NM_004181.5(UCHL1):c.45+6T>C	rs11556273	0.05228
NM_004181.5(UCHL1):c.558C>T (p.Gly186=)	rs116680633	0.00540
NM_004181.5(UCHL1):c.*309T>C	rs78683791	0.00537
NM_004181.5(UCHL1):c.*294G>A	rs116700032	0.00381
NM_004181.4(UCHL1):c.-71C>G	rs201100258	0.00108
NM_004181.5(UCHL1):c.609A>G (p.Glu203=)	rs147661219	0.00045
NM_004181.5(UCHL1):c.-16C>T	rs9321

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