List of variants in gene CDH23 reported as uncertain significance by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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.7468G>A (p.Glu2490Lys)	rs41281336	0.00035
NM_022124.6(CDH23):c.2236G>A (p.Val746Ile)	rs550384315	0.00021
NM_022124.6(CDH23):c.7343T>C (p.Phe2448Ser)

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