RS367543052 MYH7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital myopathy with fiber type disproportion
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
MYH7-related skeletal myopathy
Congenital myopathy with fiber type disproportion
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
MYH7-related skeletal myopathy
Other Variants in MYH7