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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF292
(S1909fs +1 more)
Deletion
(frameshift variant)
Intellectual developmental disorder, autosomal dominant 64
GLikely pathogenic
ZNF292
(E1914fs +1 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder
+4 more
GPathogenic/Likely pathogenic