RS587782951 JPH2

Health Risk Chr 20:44160305
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Primary familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in JPH2
rs1600482909 rs387906897 rs387906898 rs398124358 rs730880254 rs147407445 rs531877510 rs367563723 rs181096982 rs765754956
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