List of variants in gene combination CDH23, PSAP reported as benign for CDH23-related disorder

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.9903C>T (p.Pro3301=)	rs55717455	0.00341
NM_022124.6(CDH23):c.9501G>A (p.Thr3167=)	rs144906721	0.00292
NM_022124.6(CDH23):c.10026C>T (p.Asp3342=)	rs377118941	0.00185

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