RS104894369 MYL2
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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 10
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Hypertrophic cardiomyopathy 10
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Other Variants in MYL2