ClinVar Miner

List of variants in gene CDH23 reported as uncertain significance for Deafness, autosomal recessive 12

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_022124.6(CDH23):c.4405A>G (p.Ile1469Val) rs200635365
NM_022124.6(CDH23):c.4662C>A (p.Asp1554Glu) rs771353319
NM_022124.6(CDH23):c.5747G>A (p.Arg1916His) rs746971522
NM_022124.6(CDH23):c.7517G>A (p.Arg2506Gln) rs727502932
NM_022124.6(CDH23):c.8248G>A (p.Val2750Met) rs752930006

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.