ClinVar Miner

List of variants in gene TNNT2 reported as benign for Familial hypertrophic cardiomyopathy 2; Left ventricular noncompaction 6; Familial restrictive cardiomyopathy 3

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_001276345.2(TNNT2):c.200-11A>G rs368658464
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=) rs3729845
NM_001276345.2(TNNT2):c.294+7G>A rs45490292
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=) rs3729547
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.52+7G>A rs374443596
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833
NM_001276345.2(TNNT2):c.53-11_53-7del rs45533739
NM_001276345.2(TNNT2):c.68-8A>G rs115805892
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg) rs3730238

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.