ClinVar Miner

Submissions for variant NM_000069.3(CACNA1S):c.3627C>T (p.Ser1209=)

gnomAD frequency: 0.00001  dbSNP: rs200852196
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 RCV001402722 SCV001604573 likely benign Hypokalemic periodic paralysis, type 1; Malignant hyperthermia, susceptibility to, 5 2024-10-23 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006890 SCV004816676 likely benign Malignant hyperthermia, susceptibility to, 5 2023-04-27 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003953733 SCV004772139 likely benign CACNA1S-related disorder 2019-07-13 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.