List of variants in gene CDH23 reported by National Institute on Deafness and Communication Disorders, National Institutes of Health

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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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.5237G>A (p.Arg1746Gln)	rs111033270	0.00016
NM_022124.6(CDH23):c.2560C>T (p.Arg854Cys)	rs768340895	0.00004
NM_022124.6(CDH23):c.271C>T (p.Gln91Ter)	rs1853882557
NM_022124.6(CDH23):c.3176A>T (p.Asp1059Val)	rs1865887896
NM_022124.6(CDH23):c.7872+1G>A	rs746152246
NM_022124.6(CDH23):c.9726del (p.Ser3243fs)	rs767176528

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