ClinVar Miner

Submissions for variant NM_000441.2(SLC26A4):c.2049_2058del (p.Phe683fs)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003472897 SCV004201946 likely pathogenic Autosomal recessive nonsyndromic hearing loss 4 2023-04-05 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005036825 SCV005673659 likely pathogenic Autosomal recessive nonsyndromic hearing loss 4; Pendred syndrome 2024-06-14 criteria provided, single submitter clinical testing

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.