ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.6340A>G (p.Thr2114Ala)

gnomAD frequency: 0.00001  dbSNP: rs1025586071
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 RCV001203325 SCV001374484 benign Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV 2024-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002484094 SCV002791487 uncertain significance Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV 2021-11-15 criteria provided, single submitter clinical testing
Ambry Genetics RCV003284040 SCV003976621 likely benign Inborn genetic diseases 2023-04-20 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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.