RS863225117 MYL2

Health Risk Chr 12:110915759
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hypertrophic cardiomyopathy 10
Cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 10
Cardiomyopathy
Cardiovascular phenotype
Other Variants in MYL2
rs104894363 rs104894368 rs104894369 rs104894370 rs199474808 rs199474813 rs199474815 rs192057022 rs193922452 rs397516398
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