RS397516187 MYH7

Health Risk Chr 14:23419993
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Primary dilated cardiomyopathy
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Primary dilated cardiomyopathy
Other Variants in MYH7
rs121913624 rs3218713 rs121913625 rs121913626 rs121913627 rs121913628 rs121913629 rs121913630 rs121913631 rs121913632
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