RS606231332 MYH7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial cardiomyopathy
Hypertrophic cardiomyopathy
Cardiomyopathy
Cardiovascular phenotype
Familial cardiomyopathy
Hypertrophic cardiomyopathy
Cardiomyopathy
Cardiovascular phenotype
Other Variants in MYH7