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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2A
(N1029K)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
GUncertain significance
GRIN2A
(L887fs)
Deletion
(frameshift variant)
not provided
GPathogenic
GRIN2A
Single nucleotide variant
(splice acceptor variant)
not provided
GLikely pathogenic
GRIN2A
(A243V)
Single nucleotide variant
(missense variant)
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
GLikely pathogenic
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