ClinVar Miner

Submissions for variant NM_006516.2(SLC2A1):c.-424C>G

gnomAD frequency: 0.01606  dbSNP: rs867977523
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
Illumina Laboratory Services, Illumina RCV000278436 SCV000357741 uncertain significance GLUT1 deficiency syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000333448 SCV000357742 uncertain significance Dystonic disorder 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001653458 SCV001862358 benign not provided 2018-06-14 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.