List of variants in gene UCHL1 reported as likely pathogenic for not provided

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004181.5(UCHL1):c.349_364del (p.Phe117fs)	rs1781070341
NM_004181.5(UCHL1):c.385_388dup (p.Ala130fs)	rs1554004920
NM_004181.5(UCHL1):c.460-2A>G	rs2154087252
NM_004181.5(UCHL1):c.64dup (p.Val22fs)	rs1781001592

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