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

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.5237G>A (p.Arg1746Gln)	rs111033270	0.00016
NM_022124.6(CDH23):c.6442G>A (p.Asp2148Asn)	rs111033271	0.00010
NM_022124.6(CDH23):c.6050-9G>A	rs367928692	0.00006
NM_022124.6(CDH23):c.5712G>A (p.Thr1904=)	rs397517342	0.00001
NM_022124.6(CDH23):c.9381-2A>G

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