ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.568T>C (p.Trp190Arg) (rs121918773)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Bioinformatics, Peking University RCV000059548 SCV000221964 pathogenic Severe myoclonic epilepsy in infancy 2014-12-20 criteria provided, single submitter research
Neurogenetics Laboratory - MEYER, AOU Meyer RCV000059548 SCV000494511 pathogenic Severe myoclonic epilepsy in infancy 2016-11-16 criteria provided, single submitter clinical testing
UniProtKB/Swiss-Prot RCV000059548 SCV000091080 not provided Severe myoclonic epilepsy in infancy no assertion provided not provided

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.