RS2030801584 AIFM1

Health Risk Chr X:130147592
Upload your DNA to see your genotype for this variant.
Associated Conditions
Severe X-linked mitochondrial encephalomyopathy
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Severe X-linked mitochondrial encephalomyopathy
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Other Variants in AIFM1
rs387906500 rs281864468 rs724160024 rs724160022 rs724160025 rs724160021 rs724160020 rs724160026 rs184474885 rs724160018
Ask Dr. Hemsworth about this variant