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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2B
(G499R)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 6
+2 more
GLikely pathogenic
GRIN2B
(N368T)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 27
+1 more
GConflicting classifications of pathogenicity