List of variants in gene CDH23 reported as uncertain significance for Nonsyndromic genetic 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.8083G>A (p.Asp2695Asn)	rs369501114	0.00002
NM_022124.6(CDH23):c.478G>A (p.Asp160Asn)	rs1057519500	0.00001
NM_022124.6(CDH23):c.902G>A (p.Arg301Gln)	rs121908355	0.00001
NM_022124.6(CDH23):c.6866A>G (p.Asn2289Ser)	rs876657756

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