RS140234726 MFN2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Inborn genetic diseases
MFN2-related disorder
Neuropathy
hereditary motor and sensory
type 6A
Charcot-Marie-Tooth disease type 2A2
axonal
autosomal recessive
type 2a2b
Multiple symmetric lipomatosis
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Inborn genetic diseases
Other Variants in MFN2