List of variants in gene UCHL1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004181.5(UCHL1):c.513C>T (p.His171=)	rs145093131	0.00036
NM_004181.5(UCHL1):c.609A>G (p.Glu203=)	rs147661219	0.00031
NM_004181.5(UCHL1):c.315A>G (p.Lys105=)
NM_004181.5(UCHL1):c.501C>T (p.Asn167=)
NM_004181.5(UCHL1):c.648C>A (p.Ala216=)	rs781389075

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