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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2B
(M706V)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 6
+1 more
GLikely pathogenic
GRIN2B
(I695T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic