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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BCL11B
(E749fs +3 more)
Duplication
(frameshift variant)
Immunodeficiency 49
+1 more
GPathogenic
BCL11B
Single nucleotide variant
(splice donor variant)
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities
GPathogenic