ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance for Hypertrophic cardiomyopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_001276345.2(TNNT2):c.-22G>T rs886045829
NM_001276345.2(TNNT2):c.136G>C (p.Ala46Pro) rs397516447
NM_001276345.2(TNNT2):c.341C>T (p.Ala114Val) rs727504245
NM_001276345.2(TNNT2):c.522C>A (p.Asn174Lys) rs483352833
NM_001276345.2(TNNT2):c.601-8C>T rs397516475
NM_001276345.2(TNNT2):c.691A>G (p.Ile231Val) rs886045828
NM_001276345.2(TNNT2):c.720-5T>G rs730881092
NM_001276345.2(TNNT2):c.884G>A (p.Gly295Glu) rs1272169178
NM_001276345.2(TNNT2):c.886C>T (p.Arg296Cys) rs367785431

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.