List of variants in gene CDH23 reported as likely benign for Autosomal recessive nonsyndromic hearing loss 12; Usher syndrome type 1D; Pituitary adenoma 5, multiple types

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.429+18T>C	rs141451003	0.02288
NM_022124.6(CDH23):c.4846-19G>C	rs80261750	0.00835
NM_022124.6(CDH23):c.1449+76C>A	rs41281304	0.00518
NM_022124.6(CDH23):c.2263C>T (p.His755Tyr)	rs181255269	0.00078
NM_022124.6(CDH23):c.832+8A>G	rs56129333	0.00048
NM_022124.6(CDH23):c.5131G>A (p.Val1711Ile)	rs181611778	0.00007
NC_000010.11:g.71806223_71806224delinsTT	rs876657422
NM_022124.6(CDH23):c.5130C>T (p.Ile1710=)	rs111033487
NM_022124.6(CDH23):c.7113C>T (p.Thr2371=)	rs747544364
NM_022124.6(CDH23):c.8121G>T (p.Pro2707=)	rs377535432
NM_022124.6(CDH23):c.8229C>T (p.Arg2743=)	rs372996083
NM_022124.6(CDH23):c.9885C>T (p.Thr3295=)	rs1382062973

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