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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNA2
(G849V)
Single nucleotide variant
(missense variant +1 more)
Mitochondrial DNA deletion syndrome with progressive myopathy
GUncertain significance
DNA2
(R484fs)
Deletion
(frameshift variant +1 more)
Mitochondrial DNA deletion syndrome with progressive myopathy
GUncertain significance