RS184474885 AIFM1

Health Risk Chr X:130137123
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Deafness
X-linked 5
Charcot-Marie-Tooth Neuropathy X
Combined oxidative phosphorylation deficiency
Deafness
X-linked 5
Charcot-Marie-Tooth Neuropathy X
Combined oxidative phosphorylation deficiency
Other Variants in AIFM1
rs387906500 rs281864468 rs724160024 rs724160022 rs724160025 rs724160021 rs724160020 rs724160026 rs724160018 rs724160016
Ask Dr. Hemsworth about this variant