ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.14314G>A (p.Gly4772Ser)

dbSNP: rs193922622
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001841540 SCV000053082 likely pathogenic Cardiac arrhythmia 2011-08-18 criteria provided, single submitter curation Converted during submission to Likely pathogenic.

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.