RS369762154 MFN2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Charcot-Marie-Tooth disease type 2
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2A2
Inborn genetic diseases
Charcot-Marie-Tooth disease type 2
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2A2
Inborn genetic diseases
Other Variants in MFN2