List of variants in gene combination CDH23, PSAP reported as likely benign by GeneDx

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.*361C>A	rs115033851	0.00420
NM_022124.6(CDH23):c.10026C>T (p.Asp3342=)	rs377118941	0.00185
NM_022124.6(CDH23):c.9942G>A (p.Thr3314=)	rs376804660	0.00053

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