List of variants in gene CDH23 reported as uncertain significance by Department of Otolaryngology – Head & Neck Surgery, Cochlear Implant 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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.9928C>T (p.Arg3310Cys)	rs200124827	0.00018
NM_022124.6(CDH23):c.7552G>A (p.Val2518Met)	rs376617494	0.00011
NM_022124.6(CDH23):c.8534G>A (p.Arg2845His)	rs199668532	0.00009
NM_022124.6(CDH23):c.9941C>T (p.Thr3314Met)	rs559427378	0.00006
NM_022124.6(CDH23):c.5692G>A (p.Ala1898Thr)	rs548937425	0.00004
NM_022124.6(CDH23):c.5989G>A (p.Val1997Met)	rs755121910	0.00004
NM_022124.6(CDH23):c.2159G>A (p.Arg720Gln)	rs768074758	0.00002
NM_022124.6(CDH23):c.6980T>A (p.Leu2327His)	rs995094571	0.00001
NM_022124.6(CDH23):c.1129G>A (p.Asp377Asn)	rs779502033
NM_022124.6(CDH23):c.1484T>G (p.Val495Gly)	rs2132664465
NM_022124.6(CDH23):c.8299T>C (p.Phe2767Leu)	rs370903798

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.