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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC112529895, SCO1
(R47Q)
Single nucleotide variant
(missense variant)
Leigh syndrome
+3 more
GUncertain significance
LOC112529895, SCO1
(P32A)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance