List of variants in gene CDH23 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.6847G>A (p.Val2283Ile)	rs41281334	0.03832
NM_022124.6(CDH23):c.4858G>A (p.Val1620Met)	rs41281330	0.01037
NM_022124.6(CDH23):c.5985C>T (p.Tyr1995=)	rs370762205	0.00014
NM_022124.6(CDH23):c.4773G>A (p.Pro1591=)	rs376037961	0.00006
NM_022124.6(CDH23):c.5418C>G (p.Asp1806Glu)	rs74145660

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