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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIA3
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
GRIA3
(A129fs)
Duplication
(frameshift variant +1 more)
Syndromic X-linked intellectual disability 94
GBenign
GRIA3
(K389T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
GRIA3
(R394Q)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign/Likely benign
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