RS730880792 MIR208B;MYH7
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 1
Dilated cardiomyopathy 1S
MYH7-related skeletal myopathy
Myosin storage myopathy
Cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 1
Dilated cardiomyopathy 1S
MYH7-related skeletal myopathy
Myosin storage myopathy
Cardiomyopathy