RS727503278 MYH7

Health Risk Chr 14:23432714
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hypertrophic cardiomyopathy
Inborn genetic diseases
Primary familial hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 1
Cardiovascular phenotype
Hypertrophic cardiomyopathy 1
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy
Inborn genetic diseases
Primary familial hypertrophic cardiomyopathy
Cardiomyopathy
Hypertrophic cardiomyopathy 1
Cardiovascular phenotype
Other Variants in MYH7
rs121913624 rs3218713 rs121913625 rs121913626 rs121913627 rs121913628 rs121913629 rs121913630 rs121913631 rs121913632
Ask Dr. Hemsworth about this variant