RS749361266 MPV17
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What This Variant Does
"CLNSIG=4
Associated Conditions
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
Charcot-Marie-Tooth disease
axonal
type 2EE
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
Charcot-Marie-Tooth disease
axonal
type 2EE
Other Variants in MPV17