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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETBP1
(Q809*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 29
GPathogenic
SETBP1
(G1268W)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 29
GLikely pathogenic