RS751090469 CPT2

Health Risk Chr 1:53210595
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Associated Conditions
Carnitine palmitoyltransferase II deficiency
Inborn genetic diseases
Carnitine palmitoyltransferase II deficiency
Inborn genetic diseases
Other Variants in CPT2
rs74315293 rs74315294 rs28936375 rs28936376 rs28936673 rs28936674 rs74315295 rs74315296 rs74315297 rs1557713988
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