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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A26
(S41N)
Single nucleotide variant
(5 prime UTR variant +2 more)
Combined oxidative phosphorylation deficiency 28
+1 more
GBenign
SLC25A26
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
SLC25A26
(T120M +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign
SLC25A26
Single nucleotide variant
(3 prime UTR variant +1 more)
Combined oxidative phosphorylation deficiency 28
+1 more
GBenign
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