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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDUFS8
(R2C)
Single nucleotide variant
(missense variant)
Mitochondrial complex I deficiency, nuclear type 1
+4 more
GConflicting classifications of pathogenicity
NDUFS8
Single nucleotide variant
(synonymous variant)
Leigh syndrome
+3 more
GConflicting classifications of pathogenicity