List of variants in gene CDH23 reported as uncertain significance for Childhood onset hearing loss

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.3074G>A (p.Gly1025Asp)	rs143179070	0.00358
NM_022124.6(CDH23):c.5505G>A (p.Met1835Ile)	rs200786014	0.00053
NM_022124.6(CDH23):c.2560C>T (p.Arg854Cys)	rs768340895	0.00004
NM_022124.6(CDH23):c.9726del (p.Ser3243fs)	rs767176528

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