RS143139258 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
Hypertrophic cardiomyopathy 10
Cardiovascular phenotype
Dilated cardiomyopathy 1S
Primary dilated cardiomyopathy
Cardiomyopathy
Myopathy
myofibrillar
12
infantile-onset
with cardiomyopathy
Sarcoma
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 10
Cardiovascular phenotype
Other Variants in MYL2