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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLAT
(D123Y +3 more)
Single nucleotide variant
(missense variant +3 more)
not provided
+1 more
GUncertain significance
DLAT
(P192L +6 more)
Single nucleotide variant
(missense variant +1 more)
Pyruvate dehydrogenase E2 deficiency
GUncertain significance
DLAT
(T185I +7 more)
Single nucleotide variant
(missense variant +1 more)
Pyruvate dehydrogenase E2 deficiency
GUncertain significance
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