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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2A
(N976S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
GRIN2A
(A716T)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
+1 more
GPathogenic/Likely pathogenic
GRIN2A
(N615K)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
GLikely pathogenic
GRIN2A
(R518H)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
+1 more
GPathogenic/Likely pathogenic
GRIN2A
Single nucleotide variant
(splice donor variant)
Landau-Kleffner syndrome
+1 more
GPathogenic/Likely pathogenic
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