List of variants in gene CDH23 reported as uncertain significance by Clinical Genetics, Academic Medical Center

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.4405A>G (p.Ile1469Val)	rs200635365	0.00014
NM_022124.6(CDH23):c.415G>A (p.Val139Ile)	rs771868822	0.00008
NM_022124.6(CDH23):c.5117G>A (p.Arg1706His)	rs376614796	0.00002
NM_022124.6(CDH23):c.1090G>A (p.Gly364Ser)	rs767750411	0.00001
NM_022124.6(CDH23):c.4519C>T (p.Arg1507Trp)	rs760927863	0.00001
NM_022124.6(CDH23):c.5518C>T (p.Arg1840Trp)	rs145951744	0.00001
NM_022124.6(CDH23):c.3179G>A (p.Arg1060Gln)	rs536438868

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