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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH15
(S203C)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 3
GUncertain significance
CDH15
(A691S)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 3
GUncertain significance
CDH15
(E740Q)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 3
GUncertain significance
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