RS730880162 MYL3

Health Risk Chr 3:46859509
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Other Variants in MYL3
rs104893748 rs199474703 rs199474707 rs199474705 rs199474706 rs202141423 rs145520567 rs147584015 rs727505197 rs148310342
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