ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.7158C>A (p.Ile2386=)

gnomAD frequency: 0.00001  dbSNP: rs761292590
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 RCV001478655 SCV001682929 likely benign RYR1-related disorder 2023-12-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007143 SCV004820902 likely benign Malignant hyperthermia, susceptibility to, 1 2023-12-13 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV001478655 SCV005337441 likely benign RYR1-related disorder 2024-07-30 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.