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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNKSR2
(E536del +3 more)
Deletion
(inframe_deletion)
Intellectual disability, X-linked, syndromic, Houge type
GUncertain significance
CNKSR2
(R584fs +3 more)
Deletion
(frameshift variant)
Intellectual disability, X-linked, syndromic, Houge type
GPathogenic
CNKSR2
(S841R +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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