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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNTNAP2
Single nucleotide variant
(intron variant)
Intellectual disability
GLikely pathogenic
CNTNAP2
(R1016*)
Single nucleotide variant
(nonsense)
Intellectual disability
+1 more
GConflicting classifications of pathogenicity
CNTNAP2
(A1227T)
Single nucleotide variant
(missense variant)
Intellectual disability
+1 more
GUncertain significance
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