RS754386565 CPT2

Health Risk Chr 1:53211088
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Carnitine palmitoyl transferase II deficiency
neonatal form
myopathic form
severe infantile form
Encephalopathy
acute
infection-induced
susceptibility to
4
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
neonatal form
myopathic form
severe infantile form
Encephalopathy
Other Variants in CPT2
rs74315293 rs74315294 rs28936375 rs28936376 rs28936673 rs28936674 rs74315295 rs74315296 rs74315297 rs1557713988
Ask Dr. Hemsworth about this variant