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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A26
(C170Y +3 more)
Single nucleotide variant
(missense variant +1 more)
Combined oxidative phosphorylation deficiency 28
GUncertain significance
SLC25A26
(G137V +3 more)
Single nucleotide variant
(missense variant +2 more)
Combined oxidative phosphorylation deficiency 28
GUncertain significance