RS74315294 CPT2
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What This Variant Does
"minor allele should be reclassified as benign according to [OMIM:?]
Associated Conditions
Carnitine palmitoyl transferase II deficiency
myopathic form
neonatal form
Carnitine palmitoyltransferase II deficiency
severe infantile form
Inborn genetic diseases
Encephalopathy
acute
infection-induced
susceptibility to
4
Rhabdomyolysis
Abnormality of the musculature
Ovarian serous cystadenocarcinoma
Thymoma
Other Variants in CPT2