RS201745292 CPT2

Health Risk Chr 1:53210863
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Associated Conditions
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
severe infantile form
myopathic form
neonatal form
Encephalopathy
acute
infection-induced
susceptibility to
4
Inborn genetic diseases
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
severe infantile form
myopathic form
Other Variants in CPT2
rs74315293 rs74315294 rs28936375 rs28936376 rs28936673 rs28936674 rs74315295 rs74315296 rs74315297 rs1557713988
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