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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIK2
(A657T)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired language and ataxia and with or without seizures
+2 more
GPathogenic
GRIK2
(T660R)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with impaired language and ataxia and with or without seizures
+3 more
GPathogenic
GRIK2
(T660K)
Single nucleotide variant
(missense variant)
GRIK2-related neurodevelopmental disorder
GPathogenic
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