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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UBR7
(S19fs)
Duplication
(frameshift variant +1 more)
Intellectual disability, mild
GPathogenic
UBR7
(L76*)
Single nucleotide variant
(nonsense)
Li-Campeau syndrome
GLikely pathogenic
UBR7
(L288P)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay
GUncertain significance
UBR7
(Q252* +1 more)
Single nucleotide variant
(nonsense +1 more)
Li-Campeau syndrome
GLikely pathogenic
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