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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IRF2BPL
(N701fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
IRF2BPL
(S358fs)
Deletion
(frameshift variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
IRF2BPL
(E166*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GPathogenic
IRF2BPL
(Q117*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
+1 more
GLikely pathogenic
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