RS267607490 DES
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Primary dilated cardiomyopathy
Desmin-related myofibrillar myopathy
Neuromuscular disease
Cardiovascular phenotype
Dilated cardiomyopathy 1I
Neurogenic scapuloperoneal syndrome
Kaeser type
Primary familial hypertrophic cardiomyopathy
Primary dilated cardiomyopathy
Desmin-related myofibrillar myopathy
Neuromuscular disease
Cardiovascular phenotype
Dilated cardiomyopathy 1I
Neurogenic scapuloperoneal syndrome
Other Variants in DES