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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1A
Deletion
(splice donor variant)
Intellectual disability, autosomal dominant 14
GLikely pathogenic
SMARCB1
(L356fs +3 more)
Microsatellite
(frameshift variant)
not provided
+1 more
GPathogenic