RS138345244 MFN2

Health Risk Chr 1:11992557 snv missense variant
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Associated Conditions
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Optic atrophy
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Optic atrophy
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
0.2%
1kG EUR
100%
1kG SAS
100%
Other Variants in MFN2
rs28940291 rs28940292 rs28940293 rs28940294 rs28940295 rs28940296 rs119103261 rs119103262 rs119103263 rs119103264
Ask Dr. Hemsworth about this variant