RS199474808 MYL2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Premature ventricular contraction
Primary familial hypertrophic cardiomyopathy
Death in infancy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 10
Hypertrophic cardiomyopathy 1
Cardiomyopathy
Myopathy
myofibrillar
12
infantile-onset
with cardiomyopathy
Hypertrophic cardiomyopathy
Premature ventricular contraction
Primary familial hypertrophic cardiomyopathy
Other Variants in MYL2