RS772308346 AIFM1

Health Risk Chr X:130149478
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Associated Conditions
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Severe X-linked mitochondrial encephalomyopathy
Inborn genetic diseases
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Severe X-linked mitochondrial encephalomyopathy
Inborn genetic diseases
Other Variants in AIFM1
rs387906500 rs281864468 rs724160024 rs724160022 rs724160025 rs724160021 rs724160020 rs724160026 rs184474885 rs724160018
Ask Dr. Hemsworth about this variant