ClinVar Miner

List of variants in gene combination CDH23, LOC111982869 reported as uncertain significance for Usher syndrome type 1

Included ClinVar conditions (16):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
Download table as spreadsheet
NM_022124.6(CDH23):c.7999G>C (p.Asp2667His) rs200251748
NM_022124.6(CDH23):c.8009G>A (p.Ser2670Asn) rs749342092
NM_022124.6(CDH23):c.8062A>G (p.Ser2688Gly)

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.