RS147205617 SCN3B

Health Risk Chr 11:123642563
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What This Variant Does
"CLNSIG=5
Associated Conditions
Death in infancy
Cardiovascular phenotype
Cardiomyopathy
Brugada syndrome 7
SCN3B-related disorder
Death in infancy
Cardiovascular phenotype
Cardiomyopathy
Brugada syndrome 7
SCN3B-related disorder
Other Variants in SCN3B
rs121918282 rs587777557 rs587777558 rs186341159 rs770801747 rs779277447 rs771342044 rs996152549 rs368054375 rs375755770
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