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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAREM2, HADHA
(P711S)
Single nucleotide variant
(missense variant)
Mitochondrial trifunctional protein deficiency
GUncertain significance
GAREM2, HADHA
(R399*)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic/Likely pathogenic