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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2B
(P1439A)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
+1 more
GUncertain significance
GRIN2B
(F941fs)
Deletion
(frameshift variant)
Intellectual disability, autosomal dominant 6
GLikely pathogenic