RS1057517494 CPT2

Health Risk Chr 1:53197037

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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

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