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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A12
(D540N)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 39
GLikely pathogenic
SLC25A12
Copy number loss
Developmental and epileptic encephalopathy, 39
GPathogenic