List of variants in gene CDH23 reported as uncertain significance for Nonsyndromic Hearing Loss, Recessive

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.9198+13C>T	rs375384238	0.00061
NM_022124.6(CDH23):c.1621G>A (p.Glu541Lys)	rs562019725	0.00011
NM_022124.6(CDH23):c.446C>T (p.Thr149Met)	rs370947344	0.00002
NM_022124.6(CDH23):c.*117dup	rs886047145
NM_022124.6(CDH23):c.-197GAGCGGC[3]	rs527578984
NM_022124.6(CDH23):c.-197GAGCGGC[5]	rs527578984
NM_022124.6(CDH23):c.2290-13del	rs397517316
NM_022124.6(CDH23):c.3109G>A (p.Gly1037Ser)	rs886047133
NM_022124.6(CDH23):c.5727T>C (p.Thr1909=)	rs756919394
NM_022124.6(CDH23):c.7661-9C>T	rs577559462

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