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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDK13
(E595*)
Single nucleotide variant
(nonsense)
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
GPathogenic
CDK13
(W697*)
Single nucleotide variant
(nonsense)
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
GLikely pathogenic