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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOX11
(E234*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 27
GLikely pathogenic
SOX11
(P263T)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 27
GUncertain significance
SOX11
(G383C)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 27
GUncertain significance
SOX11
(W429*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 27
GPathogenic
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