RS121913628 MYH7
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What This Variant Does
"The rare minor allele of this variant is reported to be pathogenic/likely pathogenic for familial hy...
Associated Conditions
Hypertrophic cardiomyopathy 1
Hypertrophic cardiomyopathy
Cardiovascular phenotype
6 conditions
Cardiomyopathy
Left ventricular noncompaction cardiomyopathy
MYH7-related disorder
Hypertrophic cardiomyopathy 1
Hypertrophic cardiomyopathy
Cardiovascular phenotype
6 conditions
Cardiomyopathy
Left ventricular noncompaction cardiomyopathy
MYH7-related disorder
Other Variants in MYH7