RS142482143 ACTN2

Health Risk Chr 1:236739318
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Associated Conditions
Cardiovascular phenotype
Cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Dilated cardiomyopathy 1AA
Myopathy
congenital
with structured cores and z-line abnormalities
distal
6
adult-onset
autosomal dominant
ACTN2-related disorder
Cardiovascular phenotype
Cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Other Variants in ACTN2
rs121434525 rs193922635 rs1150181 rs397516562 rs397516563 rs139515659 rs376923220 rs200529923 rs200248944 rs142142718
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