RS761438840 CPT2

Health Risk Chr 1:53210727

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

Carnitine palmitoyl transferase II deficiency

neonatal form

myopathic form

severe infantile form

Other Variants in CPT2

Ask Dr. Hemsworth about this variant