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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SET
(R44fs +3 more)
Deletion
(frameshift variant)
Intellectual disability
+4 more
GPathogenic/Likely pathogenic
SET
(E62fs +3 more)
Deletion
(frameshift variant)
Intellectual disability, autosomal dominant 58
GLikely pathogenic