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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIA4
(R35Q)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with or without seizures and gait abnormalities
+1 more
GUncertain significance
GRIA4
(H114R)
Single nucleotide variant
(missense variant +1 more)
See cases
GLikely pathogenic
GRIA4
(A640T)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay
GLikely pathogenic
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