ClinVar Miner

Submissions for variant NM_177550.4(SLC13A5):c.1463T>C (p.Leu488Pro) (rs587777578)

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 RCV000128862 SCV000965784 likely pathogenic Epileptic encephalopathy, early infantile, 25 2014-01-01 criteria provided, single submitter clinical testing
OMIM RCV000128862 SCV000172716 pathogenic Epileptic encephalopathy, early infantile, 25 2014-07-03 no assertion criteria provided literature only

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.