List of variants studied for Hypertrophic cardiomyopathy 2 by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.601-32A>C	rs1104859	0.73965
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys)	rs121964857	0.00044
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr)	rs45520032	0.00015
NM_001276345.2(TNNT2):c.775G>A (p.Asp259Asn)	rs141805127	0.00001
NM_001276345.2(TNNT2):c.53-11_53-7del	rs45533739

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.