List of variants in gene combination CAV3, OXTR reported as likely benign for Congenital 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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_033337.3(CAV3):c.*645A>T	rs11476	0.42415
NM_033337.3(CAV3):c.*811C>G	rs10882	0.39333
NM_033337.3(CAV3):c.*783A>G	rs7629329	0.30735
NM_033337.3(CAV3):c.123T>C (p.Phe41=)	rs13087941	0.23875
NM_033337.3(CAV3):c.*543T>C	rs13093809	0.10412
NM_033337.3(CAV3):c.*276C>T	rs77367257	0.01623
NM_033337.3(CAV3):c.*813del	rs66667169

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.