RS397516201 MYH7
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 1
6 conditions
MYH7-related disorder
MYH7-related skeletal myopathy
Myosin storage myopathy
Dilated cardiomyopathy 1S
Myopathy
myosin storage
autosomal recessive
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in MYH7