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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDUFA10
(G306fs +1 more)
Insertion
(frameshift variant +1 more)
Mitochondrial complex 1 deficiency, nuclear type 22
GUncertain significance
NDUFA10
(H202fs)
Duplication
(frameshift variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity