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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAMK2B
Single nucleotide variant
(synonymous variant +1 more)
Intellectual disability, autosomal dominant 54
+2 more
GBenign/Likely benign
CAMK2B
Single nucleotide variant
(intron variant)
Intellectual disability, autosomal dominant 54
+1 more
GBenign/Likely benign
CAMK2B
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
CAMK2B
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
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