List of variants in gene EYA4 reported as likely pathogenic for obsolete rare genetic deafness

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
NC_000006.12:g.(?_133506020)_(133528840_?)del
NM_004100.5(EYA4):c.371-2A>C	rs876657644
NM_004100.5(EYA4):c.456_459del (p.Ser153fs)	rs1583345314

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