List of variants in gene CDH23 reported as uncertain significance by Clinical Genetics Laboratory, Skane University Hospital Lund

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.8311G>A (p.Gly2771Ser)	rs201076440	0.00039
NM_022124.6(CDH23):c.2008A>T (p.Thr670Ser)	rs1304555485	0.00001
NM_022124.6(CDH23):c.3106+12dup
NM_022124.6(CDH23):c.4571del (p.Pro1524fs)
NM_022124.6(CDH23):c.4781G>T (p.Arg1594Leu)
NM_022124.6(CDH23):c.6743G>A (p.Arg2248Gln)
NM_022124.6(CDH23):c.7849G>C (p.Gly2617Arg)	rs369379727

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