RS104894368 MYL2
Upload your DNA to see your genotype for this variant.
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
Death in early adulthood
Hypertrophic cardiomyopathy
Cardiomyopathy
Cardiovascular phenotype
MYL2-related disorder
Hypertrophic cardiomyopathy 10
Death in early adulthood
Hypertrophic cardiomyopathy
Cardiomyopathy
Cardiovascular phenotype
MYL2-related disorder
Other Variants in MYL2