RS74315296 CPT2

Health Risk Chr 1:53211181
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Carnitine palmitoyl transferase II deficiency
myopathic form
Carnitine palmitoyltransferase II deficiency
neonatal form
severe infantile form
Encephalopathy
acute
infection-induced
susceptibility to
4
CPT2-related disorder
Carnitine palmitoyl transferase II deficiency
myopathic form
Carnitine palmitoyltransferase II deficiency
neonatal form
Other Variants in CPT2
rs74315293 rs74315294 rs28936375 rs28936376 rs28936673 rs28936674 rs74315295 rs74315297 rs1557713988 rs74315298
Ask Dr. Hemsworth about this variant