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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MPV17
(P139fs)
Duplication
(frameshift variant)
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
GPathogenic
MPV17
(Y135N)
Single nucleotide variant
(missense variant)
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
GUncertain significance