List of variants in gene USH1C reported as likely 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_153676.4(USH1C):c.308G>A (p.Arg103His)	rs397514500	0.00006
NM_153676.4(USH1C):c.311G>A (p.Gly104Asp)	rs1317951509	0.00001
NM_153676.4(USH1C):c.92G>A (p.Arg31Gln)	rs776511246	0.00001
NP_005700.2(USH1C):p.Arg357Trp

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