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: 13
Download table as spreadsheet
HGVS dbSNP
NM_000364.4(TNNT2):c.-1C>A rs776936911
NM_000364.4(TNNT2):c.-22G>C rs886045829
NM_000364.4(TNNT2):c.-22G>T rs886045829
NM_000364.4(TNNT2):c.233+6T>C rs397516449
NM_000364.4(TNNT2):c.270C>G (p.Pro90=) rs140245123
NM_000364.4(TNNT2):c.52+7G>A rs374443596
NM_000364.4(TNNT2):c.601-380C>T rs397516475
NM_000364.4(TNNT2):c.682A>G (p.Ile228Val) rs886045828
NM_000364.4(TNNT2):c.683T>C (p.Ile228Thr) rs45520032
NM_000364.4(TNNT2):c.711-5T>G rs730881092
NM_000364.4(TNNT2):c.711-9C>A rs763204242
NM_000364.4(TNNT2):c.875G>A (p.Gly292Glu) rs1272169178
NM_000364.4(TNNT2):c.877C>T (p.Arg293Cys) 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.