RS781186692 AIFM1
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Associated Conditions
Spondyloepimetaphyseal dysplasia
Bieganski type
Charcot-Marie-Tooth Neuropathy X
Combined oxidative phosphorylation deficiency
Spondyloepimetaphyseal dysplasia
Bieganski type
Charcot-Marie-Tooth Neuropathy X
Combined oxidative phosphorylation deficiency
Other Variants in AIFM1