List of variants in gene CDH23 reported as uncertain significance by AiLife Diagnostics, AiLife Diagnostics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.9566G>A (p.Arg3189Gln)	rs727502936	0.00004
NM_022124.6(CDH23):c.3146A>G (p.Asp1049Gly)	rs752395991	0.00003
NM_022124.6(CDH23):c.-137G>A	rs1197763355	0.00001
NM_022124.6(CDH23):c.7807G>A (p.Asp2603Asn)	rs780640943

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