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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2A
(R695Q)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder
+1 more
GPathogenic/Likely pathogenic
GRIN2A
(T690M)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
+2 more
GConflicting classifications of pathogenicity
GRIN2A
(W609C)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder
GUncertain significance
GRIN2A
(R504Q)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder
GUncertain significance
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