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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTNNB1
(Y299F +1 more)
Single nucleotide variant
(missense variant)
Severe intellectual disability-progressive spastic diplegia syndrome
GUncertain significance
CTNNB1
(R661* +1 more)
Single nucleotide variant
(nonsense)
Global developmental delay
+3 more
GPathogenic/Likely pathogenic