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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KAT6A
(S1286fs)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
KAT6A
(S378*)
Single nucleotide variant
(nonsense)
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
GPathogenic