ClinVar Miner

Submissions for variant NM_003042.4(SLC6A1):c.828C>T (p.Phe276=)

gnomAD frequency: 0.00001  dbSNP: rs1176975543
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
Labcorp Genetics (formerly Invitae), Labcorp RCV005058016 SCV002378179 likely benign Epilepsy with myoclonic atonic seizures 2023-10-06 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002219140 SCV002496781 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing SLC6A1: BP4, BP7

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.