RS201711375 AIFM1

Health Risk Chr X:130156540
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Associated Conditions
Inborn genetic diseases
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Charcot-Marie-Tooth disease X-linked recessive 4
Deafness
X-linked 5
Severe X-linked mitochondrial encephalomyopathy
Inborn genetic diseases
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Charcot-Marie-Tooth disease X-linked recessive 4
Deafness
X-linked 5
Severe X-linked mitochondrial encephalomyopathy
Other Variants in AIFM1
rs387906500 rs281864468 rs724160024 rs724160022 rs724160025 rs724160021 rs724160020 rs724160026 rs184474885 rs724160018
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