RS397516127 MYH7
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What This Variant Does
"CLNSIG=255
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
Myopathy
myosin storage
autosomal recessive
Dilated cardiomyopathy 1S
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy 1
Myosin storage myopathy
Congenital myopathy with fiber type disproportion
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 1
Other Variants in MYH7