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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIA3
(E179G)
Single nucleotide variant
(missense variant)
Syndromic X-linked intellectual disability 94
GUncertain significance
GRIA3
(G803E)
Single nucleotide variant
(missense variant +1 more)
Syndromic X-linked intellectual disability 94
+1 more
GConflicting classifications of pathogenicity