List of variants in gene CDH23 reported as likely pathogenic for Rare genetic deafness

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.6442G>A (p.Asp2148Asn)	rs111033271	0.00010
NM_022124.6(CDH23):c.7362G>A (p.Thr2454=)	rs370983472	0.00006
NM_022124.6(CDH23):c.1369C>T (p.Arg457Trp)	rs727504455	0.00001
NM_022124.6(CDH23):c.3016G>A (p.Glu1006Lys)	rs745571683	0.00001
NM_022124.6(CDH23):c.5712G>A (p.Thr1904=)	rs397517342	0.00001
NM_022124.6(CDH23):c.6049G>A (p.Gly2017Ser)	rs183431253	0.00001
NC_000010.11:g.71645936_71645956del	rs397517305
NM_022124.6(CDH23):c.2701G>A (p.Glu901Lys)	rs876657636
NM_022124.6(CDH23):c.380A>G (p.Asp127Gly)	rs876657754
NM_022124.6(CDH23):c.6412del (p.Glu2138fs)	rs111033473

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