RS730880159 MYH7
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Primary familial hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in MYH7