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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MT-ND2
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND2
Single nucleotide variant
Leigh syndrome due to mitochondrial complex I deficiency
GPathogenic
MT-ND2
Single nucleotide variant
Mitochondrial disease
GUncertain significance
MT-ATP6, MT-ATP8
+24 more
Single nucleotide variant
Mitochondrial disease
GPathogenic
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