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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNOT3
(A237V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CNOT3
(P320L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CNOT3
Deletion
(inframe_deletion)
Intellectual disability
GLikely benign
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