List of variants reported as pathogenic for heart conduction 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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.5347G>A (p.Glu1783Lys)	rs137854601	0.00001
NM_001035.3(RYR2):c.1258C>T (p.Arg420Trp)	rs190140598	0.00001
NM_000335.5(SCN5A):c.1603C>T (p.Arg535Ter)	rs1417036453
NM_000335.5(SCN5A):c.1936del (p.Gln646fs)	rs727505158
NM_000335.5(SCN5A):c.2466G>A (p.Trp822Ter)	rs1553700699
NM_000335.5(SCN5A):c.3992del (p.Pro1331fs)	rs727504801
NM_000335.5(SCN5A):c.4864C>T (p.Arg1622Ter)	rs137854613
NM_001035.3(RYR2):c.1298T>C (p.Leu433Pro)	rs121918602

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.