ClinVar Miner

Submissions for variant NM_006950.3(SYN1):c.1001del (p.Asn334fs)

dbSNP: rs1603051674
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
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne RCV001027689 SCV001190261 pathogenic Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders 2019-05-21 criteria provided, single submitter clinical testing
Institute for Human Genetics, University Hospital Essen RCV001027689 SCV002558882 pathogenic Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders 2022-07-30 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.