RS397516457 TNNT2

Health Risk Chr 1:201365291
Upload your DNA to see your genotype for this variant.
What This Variant Does
"The rare minor allele of this variant is reported to be pathogenic/likely pathogenic for familial hy...
Associated Conditions
Hypertrophic cardiomyopathy
Dilated cardiomyopathy 1D
Hypertrophic cardiomyopathy 2
Cardiomyopathy
familial restrictive
3
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Dilated cardiomyopathy 1D
Hypertrophic cardiomyopathy 2
Cardiomyopathy
familial restrictive
3
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Other Variants in TNNT2
rs121964855 rs121964856 rs121964858 rs74315379 rs74315380 rs121964860 rs193922620 rs377474357 rs397516447 rs397516448
Ask Dr. Hemsworth about this variant