RS80356779 CPT1A

Health Risk Chr 11:68780662
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What This Variant Does
"[OMIM:?]
Associated Conditions
Carnitine palmitoyl transferase 1A deficiency
CPT1A ARCTIC VARIANT
CPT1A POLYMORPHISM
CPT1A-related disorder
Inborn genetic diseases
Carnitine palmitoyl transferase 1A deficiency
CPT1A ARCTIC VARIANT
CPT1A POLYMORPHISM
CPT1A-related disorder
Inborn genetic diseases
Other Variants in CPT1A
rs80356778 rs80356787 rs80356774 rs1169875761 rs80356790 rs80356791 rs80356798 rs28936374 rs80356800 rs80356780
Ask Dr. Hemsworth about this variant