RS1553169720 CPT2

Health Risk Chr 1:53210695
Upload your DNA to see your genotype for this variant.
Associated Conditions
Carnitine palmitoyl transferase II deficiency
severe infantile form
Encephalopathy
acute
infection-induced
susceptibility to
4
neonatal form
myopathic form
Carnitine palmitoyl transferase II deficiency
severe infantile form
Encephalopathy
acute
infection-induced
susceptibility to
Other Variants in CPT2
rs74315293 rs74315294 rs28936375 rs28936376 rs28936673 rs28936674 rs74315295 rs74315296 rs74315297 rs1557713988
Ask Dr. Hemsworth about this variant