ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.5839+10G>A

gnomAD frequency: 0.00001  dbSNP: rs371733571
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 RCV001440062 SCV001642965 likely benign Episodic ataxia type 2; Developmental and epileptic encephalopathy, 42 2023-06-05 criteria provided, single submitter clinical testing
Athena Diagnostics RCV001664880 SCV001880245 uncertain significance not provided 2020-12-15 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003985497 SCV004713061 likely benign CACNA1A-related disorder 2021-12-30 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.