ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.219G>C (p.Thr73=)

gnomAD frequency: 0.00004  dbSNP: rs781239273
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001402792 SCV001604647 likely benign Episodic ataxia type 2; Developmental and epileptic encephalopathy, 42 2023-12-30 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587153 SCV005077581 likely benign not specified 2024-04-18 criteria provided, single submitter clinical testing

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.