List of variants in gene USH1C reported as pathogenic for Usher syndrome type 1

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_153676.4(USH1C):c.2014-1G>A	rs150567427	0.00183
NM_153676.4(USH1C):c.497-2del	rs1480243085	0.00001
NM_153676.4(USH1C):c.238dup (p.Arg80fs)	rs397515359

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