RS863224967 MFN2

Health Risk Chr 1:12002069
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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
MFN2-related disorder
Hereditary neuropathy or pain disorder
Charcot-Marie-Tooth disease type 2
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2A2
Inborn genetic diseases
MFN2-related disorder
Hereditary neuropathy or pain disorder
Other Variants in MFN2
rs28940291 rs28940292 rs28940293 rs28940294 rs28940295 rs28940296 rs119103261 rs119103262 rs119103263 rs119103264
Ask Dr. Hemsworth about this variant