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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2B
(S1403C)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 27
GUncertain significance
GRIN2B
(R847*)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 27
+2 more
GPathogenic/Likely pathogenic