RS119103268 MFN2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2A2
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease type 2
axonal
autosomal recessive
type 2a2b
Inborn genetic diseases
Neuropathy
hereditary motor and sensory
type 6A
Charcot-Marie-Tooth disease dominant intermediate B
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2A2
Charcot-Marie-Tooth disease
Other Variants in MFN2