RS397516171 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
Cardiovascular phenotype
6 conditions
Hypertrophic cardiomyopathy
Cardiomyopathy
Dilated cardiomyopathy 1S
Myopathy
myosin storage
autosomal recessive
Myosin storage myopathy
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy 1
Cardiovascular phenotype
MYH7-related disorder
Hypertrophic cardiomyopathy
Other Variants in MYH7