RS397516408 MYL2

Health Risk Chr 12:110919117
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 10
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy 10
Other Variants in MYL2
rs104894363 rs104894368 rs104894369 rs104894370 rs199474808 rs199474813 rs199474815 rs192057022 rs193922452 rs397516398
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