List of variants in gene CDH23 reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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: 6

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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.7723G>A (p.Glu2575Lys)	rs762925264	0.00001
NM_022124.6(CDH23):c.2171G>C (p.Arg724Pro)	rs374955091
NM_022124.6(CDH23):c.2337_2339del (p.Lys779_Asp780delinsAsn)
NM_022124.6(CDH23):c.4693TAC[1] (p.Tyr1566del)
NM_022124.6(CDH23):c.9058_9060del (p.Arg3020del)	rs786205612

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