ClinVar Miner

Submissions for variant NM_002103.5(GYS1):c.984C>T (p.Ile328=)

gnomAD frequency: 0.00003  dbSNP: rs769000809
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002140250 SCV002457857 likely benign Glycogen storage disease due to muscle and heart glycogen synthase deficiency 2021-04-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704797 SCV005209805 likely benign not provided criteria provided, single submitter not provided
PreventionGenetics, part of Exact Sciences RCV003895952 SCV004715562 likely benign GYS1-related disorder 2020-12-31 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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.