RS376598131 MFN2

Health Risk Chr 1:12005744
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Associated Conditions
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Inborn genetic diseases
MFN2-related disorder
Hereditary ataxia
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Inborn genetic diseases
MFN2-related disorder
Hereditary ataxia
Other Variants in MFN2
rs28940291 rs28940292 rs28940293 rs28940294 rs28940295 rs28940296 rs119103261 rs119103262 rs119103263 rs119103264
Ask Dr. Hemsworth about this variant