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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNOT3
(K50del)
Microsatellite
(inframe_deletion)
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies
GLikely pathogenic
CNOT3
(E51del)
Deletion
(inframe_deletion)
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies
GUncertain significance