RS397516406 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
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Other Variants in MYL2