List of variants reported as likely pathogenic for cardiac rhythm disease by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001035.2(RYR2):c.(?_169)_(273_?)del
NM_001035.3(RYR2):c.12544G>C (p.Glu4182Gln)	rs397516508
NM_001035.3(RYR2):c.506G>A (p.Arg169Gln)	rs397516539
NM_001035.3(RYR2):c.7159G>A (p.Ala2387Thr)	rs794728753
NM_001232.4(CASQ2):c.578_580delinsAC (p.Ile193fs)	rs397516643
NM_001232.4(CASQ2):c.940-1G>T	rs876657635

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.