List of variants in gene CDH23 reported as likely pathogenic for CDH23-related disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.3016G>A (p.Glu1006Lys)	rs745571683	0.00001
NM_022124.6(CDH23):c.6049G>A (p.Gly2017Ser)	rs183431253	0.00001
NM_022124.6(CDH23):c.1950del (p.Leu651fs)
NM_022124.6(CDH23):c.6713-1G>A

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