RS587782962 MYH7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
Myopathy
myosin storage
autosomal recessive
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy 1
Myosin storage myopathy
Dilated cardiomyopathy 1S
See cases
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in MYH7