List of variants in gene CDH23 reported as uncertain significance for 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
NM_022124.6(CDH23):c.7823G>A (p.Arg2608His)	rs202052174	0.00059
NM_022124.6(CDH23):c.2104C>T (p.Arg702Trp)	rs528779319	0.00001
NM_022124.6(CDH23):c.6614C>T (p.Pro2205Leu)	rs397517349	0.00001

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