ClinVar Miner

Submissions for variant NM_177559.3(CSNK2A1):c.62G>A (p.Arg21Gln)

gnomAD frequency: 0.00001  dbSNP: rs1402734448
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences RCV001728099 SCV001548578 uncertain significance Okur-Chung neurodevelopmental syndrome 2021-03-10 no assertion criteria provided 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.