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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PHF21A
(K391* +1 more)
Single nucleotide variant
(nonsense +1 more)
Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures
+1 more
GPathogenic
PHF21A
(T272fs +1 more)
Deletion
(frameshift variant +1 more)
Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures
GPathogenic
PHF21A
Single nucleotide variant
(splice acceptor variant +1 more)
Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures
GLikely pathogenic
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