RS397516166 MYH7
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Other Variants in MYH7