RS397516220 MYH7

Health Risk Chr 14:23416988
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What This Variant Does
"CLNSIG=5
Associated Conditions
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
Congenital myopathy
MYH7-related skeletal myopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
Congenital myopathy
Other Variants in MYH7
rs121913624 rs3218713 rs121913625 rs121913626 rs121913627 rs121913628 rs121913629 rs121913630 rs121913631 rs121913632
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