ClinVar Miner

List of variants in gene CDH23 reported as pathogenic by Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.8920G>T (p.Glu2974Ter)	rs1344509500	0.00001
NM_022124.6(CDH23):c.5369-1G>T	rs1564791773

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