RS397516470 TNNT2
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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
Hypertrophic cardiomyopathy 2
Dilated cardiomyopathy 1D
Cardiomyopathy
familial restrictive
3
Cardiovascular phenotype
Cardiomyopathy
familial restrictive
3
Dilated cardiomyopathy 1D
Hypertrophic cardiomyopathy 2
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 2
Dilated cardiomyopathy 1D
Other Variants in TNNT2