RS28936673 CPT2

Health Risk Chr 1:53213501
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What This Variant Does
"[OMIM:CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE]
Associated Conditions
Carnitine palmitoyl transferase II deficiency
severe infantile form
Carnitine palmitoyltransferase II deficiency
myopathic form
neonatal form
Carnitine palmitoyl transferase II deficiency
severe infantile form
Carnitine palmitoyltransferase II deficiency
myopathic form
neonatal form
Other Variants in CPT2
rs74315293 rs74315294 rs28936375 rs28936376 rs28936674 rs74315295 rs74315296 rs74315297 rs1557713988 rs74315298
Ask Dr. Hemsworth about this variant