ClinVar Miner

Submissions for variant NM_001367721.1(CASK):c.432C>T (p.Pro144=)

gnomAD frequency: 0.00012  dbSNP: rs761142771
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
Invitae RCV000950925 SCV001097270 benign Intellectual disability, CASK-related, X-linked 2024-01-27 criteria provided, single submitter clinical testing
GeneDx RCV001593143 SCV001825116 likely benign not provided 2020-10-13 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.