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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUX2
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GBenign/Likely benign
CUX2
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
CUX2
Single nucleotide variant
(synonymous variant)
Developmental and epileptic encephalopathy, 67
+1 more
GBenign/Likely benign
CUX2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
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