ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.1891G>T (p.Val631Phe)

dbSNP: rs2133060549
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
Genome-Nilou Lab RCV001578647 SCV001805909 uncertain significance Autosomal recessive nonsyndromic hearing loss 23 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578648 SCV001805910 uncertain significance Usher syndrome type 1F 2021-07-14 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.