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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNKSR2
Single nucleotide variant
(splice acceptor variant)
Intellectual disability
GUncertain significance
CNKSR2
Single nucleotide variant
(splice acceptor variant)
Intellectual disability
GPathogenic
CNKSR2
(S943F +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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