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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETBP1
(K160E)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 29
+1 more
GUncertain significance
SETBP1
(G872R)
Single nucleotide variant
(missense variant)
Atrial septal defect
+7 more
GLikely pathogenic
SETBP1
(Y1066*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 29
GPathogenic
SETBP1
(G1114A)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 29
GUncertain significance
SETBP1
(T1387M)
Single nucleotide variant
(missense variant)
Macrocephaly
+6 more
GConflicting classifications of pathogenicity
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