RS202219398 AIFM1

Health Risk Chr X:130133373
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What This Variant Does
"CLNSIG=4
Associated Conditions
Charcot-Marie-Tooth disease X-linked recessive 4
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Tip-toe gait
Charcot-Marie-Tooth disease X-linked recessive 4
Combined oxidative phosphorylation deficiency
Charcot-Marie-Tooth Neuropathy X
Tip-toe gait
Other Variants in AIFM1
rs387906500 rs281864468 rs724160024 rs724160022 rs724160025 rs724160021 rs724160020 rs724160026 rs184474885 rs724160018
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