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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IRF2BPL, LOC107984638
Microsatellite
(inframe_deletion)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance
IRF2BPL, LOC107984638
(D18E)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
GUncertain significance