RS202141173 MYH7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 1
Primary familial hypertrophic cardiomyopathy
Cardiomyopathy
Cardiovascular phenotype
6 conditions
MYH7-related disorder
Myopathy
myosin storage
autosomal recessive
MYH7-related skeletal myopathy
Myosin storage myopathy
Dilated cardiomyopathy 1S
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 1
Other Variants in MYH7