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

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.1449+74G>T	rs115450602	0.00906
NM_022124.6(CDH23):c.1134+22C>T	rs115745871	0.00690
NM_022124.6(CDH23):c.2337G>A (p.Lys779=)	rs111033461	0.00664
NM_022124.6(CDH23):c.3074G>A (p.Gly1025Asp)	rs143179070	0.00358
NM_022124.6(CDH23):c.5419G>A (p.Val1807Met)	rs143993990	0.00265
NM_022124.6(CDH23):c.1307G>A (p.Ser436Asn)	rs111033369	0.00248
NM_022124.6(CDH23):c.4842G>C (p.Leu1614=)	rs368377560	0.00236
NM_022124.6(CDH23):c.6713-8G>A	rs369946986	0.00176
NM_022124.6(CDH23):c.6197G>A (p.Arg2066Gln)	rs201887949	0.00010
NM_022124.6(CDH23):c.5660C>T (p.Thr1887Ile)	rs397517340	0.00003

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