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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIA3
(R450*)
Single nucleotide variant
(nonsense)
Syndromic X-linked intellectual disability 94
+2 more
GConflicting classifications of pathogenicity
GRIA3
(G492S)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
GRIA3
(G630R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
GRIA3
(L859F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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