RS147136530 MFN2

Health Risk Chr 1:12001426
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
axonal
autosomal recessive
type 2a2b
Inborn genetic diseases
Optic atrophy
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
axonal
autosomal recessive
type 2a2b
Inborn genetic diseases
Other Variants in MFN2
rs28940291 rs28940292 rs28940293 rs28940294 rs28940295 rs28940296 rs119103261 rs119103262 rs119103263 rs119103264
Ask Dr. Hemsworth about this variant