ClinVar Miner

List of variants in gene CDH23 reported as uncertain significance by Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.9670C>T (p.Arg3224Trp)	rs111033457	0.00106
NM_022124.6(CDH23):c.1282G>A (p.Asp428Asn)	rs188376296	0.00009

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