ClinVar Miner

Submissions for variant NM_006516.4(SLC2A1):c.19-4G>A

gnomAD frequency: 0.00001  dbSNP: rs398124229
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
Eurofins Ntd Llc (ga) RCV000081429 SCV000113360 uncertain significance not provided 2013-05-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002514435 SCV003268123 likely benign GLUT1 deficiency syndrome 1, autosomal recessive 2023-07-18 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.