RS104894370 MYL2

Health Risk Chr 12:110919145
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypertrophic cardiomyopathy 10
Cardiovascular phenotype
Myopathy
myofibrillar
12
infantile-onset
with cardiomyopathy
Hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Cardiovascular phenotype
Myopathy
myofibrillar
12
infantile-onset
Other Variants in MYL2
rs104894363 rs104894368 rs104894369 rs199474808 rs199474813 rs199474815 rs192057022 rs193922452 rs397516398 rs397516399
Ask Dr. Hemsworth about this variant