ClinVar Miner

List of variants in gene SLC37A4 reported as likely benign for Glycogen storage disease, type I

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
Download table as spreadsheet
NM_001164277.1(SLC37A4):c.149-14A>G rs79849261
NM_001164277.1(SLC37A4):c.183T>C (p.Ala61=) rs34123220

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.