RS397516209 MYH7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 1
Hypertrophic cardiomyopathy
Cardiovascular phenotype
6 conditions
Cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiomyopathy
Dilated cardiomyopathy 1S
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy 1
Myopathy
myosin storage
Other Variants in MYH7