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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A22
(L194R)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 3
GUncertain significance
SLC25A22
(A32P)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 3
GUncertain significance