List of variants in gene CAV3 reported as likely benign for Long QT syndrome

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

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_033337.3(CAV3):c.40G>A (p.Val14Ile)	rs121909281	0.00088
NM_033337.3(CAV3):c.39C>T (p.Ile13=)	rs200562715	0.00006
NM_033337.3(CAV3):c.30G>A (p.Glu10=)	rs587780883	0.00002
NM_033337.3(CAV3):c.114+11C>T	rs779911803	0.00001
NM_033337.3(CAV3):c.60G>A (p.Lys20=)	rs972788554	0.00001
NM_033337.3(CAV3):c.114+16C>T
NM_033337.3(CAV3):c.114+8C>G	rs987275270
NM_033337.3(CAV3):c.27C>G (p.Leu9=)	rs1974763
NM_033337.3(CAV3):c.54C>T (p.His18=)	rs775054657
NM_033337.3(CAV3):c.63G>A (p.Glu21=)	rs1417709772
NM_033337.3(CAV3):c.9A>G (p.Ala3=)	rs2124977096

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.