RS1566147422 MYL2
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Associated Conditions
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Congenital myopathy with fiber type disproportion
Myopathy
myofibrillar
12
infantile-onset
with cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Congenital myopathy with fiber type disproportion
Myopathy
myofibrillar
Other Variants in MYL2