RS119103264 MFN2

Health Risk Chr 1:12001411
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2A2
Inborn genetic diseases
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2A2
Inborn genetic diseases
Other Variants in MFN2
rs28940291 rs28940292 rs28940293 rs28940294 rs28940295 rs28940296 rs119103261 rs119103262 rs119103263 rs119103265
Ask Dr. Hemsworth about this variant