RS373714948 CPT2

Health Risk Chr 1:53213582
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Associated Conditions
Carnitine palmitoyltransferase II deficiency
Inborn genetic diseases
Carnitine palmitoyl transferase II deficiency
severe infantile form
myopathic form
neonatal form
Encephalopathy
acute
infection-induced
susceptibility to
4
Carnitine palmitoyltransferase II deficiency
Inborn genetic diseases
Carnitine palmitoyl transferase II deficiency
severe infantile form
Other Variants in CPT2
rs74315293 rs74315294 rs28936375 rs28936376 rs28936673 rs28936674 rs74315295 rs74315296 rs74315297 rs1557713988
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