List of variants in gene USH2A reported as pathogenic for Hearing impairment

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_206933.4(USH2A):c.11864G>A (p.Trp3955Ter)	rs111033364	0.00013
NM_206933.4(USH2A):c.908G>A (p.Arg303His)	rs371777049	0.00004
NM_206933.4(USH2A):c.2168-1G>C	rs748961218	0.00001

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