List of variants in gene USH1C reported as pathogenic for Usher syndrome type 1C; Autosomal recessive nonsyndromic hearing loss 18A; Usher syndrome type 1

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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.216G>A (p.Val72=)	rs151045328	0.00002
NM_153676.4(USH1C):c.91C>T (p.Arg31Ter)	rs121908370	0.00001
NM_153676.4(USH1C):c.496+1G>T	rs138138689

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