List of variants in gene GSDME reported as likely pathogenic for autosomal dominant nonsyndromic hearing loss

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_001127453.2(GSDME):c.1183+5G>A	rs777359423
NM_001127453.2(GSDME):c.1274ATG[1] (p.Asp426del)	rs374353052
NM_001127453.2(GSDME):c.212-1G>A	rs1790597003

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