RS371898076 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
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 1
Cardiovascular phenotype
MYH7-related skeletal myopathy
Myopathy
myosin storage
autosomal recessive
Myosin storage myopathy
Dilated cardiomyopathy 1S
6 conditions
Cardiomyopathy
MYH7-related disorder
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Other Variants in MYH7