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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN1
(F589L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRIN1
(R844C +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 8
+4 more
GPathogenic/Likely pathogenic