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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CIC
(F1310L +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 45
GUncertain significance
CIC
(G1425R +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 45
GUncertain significance
CIC
(A1253S +2 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 45
GUncertain significance
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