List of variants in gene CDH23 reported as uncertain significance by Laboratory of Prof. Karen Avraham, Tel Aviv University

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.1276C>T (p.Arg426Cys)	rs373674747	0.00001
NM_022124.6(CDH23):c.2863C>A (p.Arg955Ser)	rs765094120
NM_022124.6(CDH23):c.6532A>T (p.Ile2178Phe)
NM_022124.6(CDH23):c.7849G>C (p.Gly2617Arg)	rs369379727

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