ClinVar Miner

Submissions for variant NM_001330260.2(SCN8A):c.5847T>C (p.Ser1949=)

gnomAD frequency: 0.00001  dbSNP: rs751637843
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
CeGaT Center for Human Genetics Tuebingen RCV000871600 SCV001148747 uncertain significance not provided 2019-05-01 criteria provided, single submitter clinical testing
Invitae RCV001495223 SCV001699895 likely benign Early infantile epileptic encephalopathy with suppression bursts 2021-04-10 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.