ClinVar Miner

List of variants reported as likely pathogenic for Familial hypertrophic cardiomyopathy 2

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_000364.4(TNNT2):c.653T>C (p.Ile218Thr) rs863225120
NM_000364.4(TNNT2):c.842+1G>C rs111377893
NM_001276345.2(TNNT2):c.305G>A (p.Arg102Gln) rs121964856
NM_001276345.2(TNNT2):c.566C>T (p.Ser189Phe) rs727504246
NM_001276345.2(TNNT2):c.842A>T (p.Asn281Ile) rs863225119
NM_001276345.2(TNNT2):c.890G>A (p.Trp297Ter) rs727504247

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.