RS730880852 MYH7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Myopathy
myosin storage
autosomal recessive
Hypertrophic cardiomyopathy 1
MYH7-related skeletal myopathy
Dilated cardiomyopathy 1S
Hypertrophic cardiomyopathy
Myosin storage myopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
6 conditions
Cardiomyopathy
Myopathy
myosin storage
autosomal recessive
Other Variants in MYH7