List of variants in gene CDH23 reported as likely benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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.6852G>C (p.Leu2284=)	rs56013867	0.00491
NM_022124.6(CDH23):c.1307G>A (p.Ser436Asn)	rs111033369	0.00248
NM_022124.6(CDH23):c.2263C>T (p.His755Tyr)	rs181255269	0.00078
NM_022124.6(CDH23):c.2572G>A (p.Val858Ile)	rs181275139	0.00023

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