RS28936376 CPT2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET]
Associated Conditions
Carnitine palmitoyl transferase II deficiency
myopathic form
severe infantile form
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
myopathic form
severe infantile form
Carnitine palmitoyltransferase II deficiency
Other Variants in CPT2