RS192057022 MYL2

Health Risk Chr 12:110913139
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 10
Cardiovascular phenotype
Cardiomyopathy
Myopathy
myofibrillar
12
infantile-onset
with cardiomyopathy
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 10
Cardiovascular phenotype
Cardiomyopathy
Myopathy
Other Variants in MYL2
rs104894363 rs104894368 rs104894369 rs104894370 rs199474808 rs199474813 rs199474815 rs193922452 rs397516398 rs397516399
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