RS104894363 MYL2

Health Risk Chr 12:110919160
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypertrophic cardiomyopathy 10
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 1
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 10
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 1
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Cardiomyopathy
Other Variants in MYL2
rs104894368 rs104894369 rs104894370 rs199474808 rs199474813 rs199474815 rs192057022 rs193922452 rs397516398 rs397516399
Ask Dr. Hemsworth about this variant