RS368900406 MPV17;TRIM54;UCN
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Associated Conditions
MPV17-related mitochondrial DNA maintenance defect
Charcot-Marie-Tooth disease
axonal
type 2EE
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
MPV17-related mitochondrial DNA maintenance defect
Charcot-Marie-Tooth disease
axonal
type 2EE
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)