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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOX11
(R64C)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 27
GLikely pathogenic
SOX11
(E296*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 27
GLikely pathogenic