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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OXCT1
(T271I +4 more)
Single nucleotide variant
(missense variant +1 more)
Succinyl-CoA acetoacetate transferase deficiency
GPathogenic
OXCT1
Single nucleotide variant
(intron variant)
not specified
+1 more
GLikely benign