RS769239899 ACTN2
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Associated Conditions
Dilated cardiomyopathy 1AA
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Myopathy
congenital
with structured cores and z-line abnormalities
distal
6
adult-onset
autosomal dominant
ACTN2-related disorder
Dilated cardiomyopathy 1AA
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Myopathy
Other Variants in ACTN2