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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAMK2B
(E330Q +6 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 54
+1 more
GUncertain significance
CAMK2B
Single nucleotide variant
(intron variant +1 more)
Intellectual disability, autosomal dominant 54
+1 more
GUncertain significance
CAMK2B
Single nucleotide variant
(intron variant)
Intellectual disability, autosomal dominant 54
GUncertain significance
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