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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSNK2B
Single nucleotide variant
(splice acceptor variant)
Poirier-Bienvenu neurodevelopmental syndrome
GPathogenic/Likely pathogenic
CSNK2B
(R111P)
Single nucleotide variant
(missense variant)
Poirier-Bienvenu neurodevelopmental syndrome
GPathogenic
CSNK2B
(L184R +1 more)
Single nucleotide variant
(missense variant)
Poirier-Bienvenu neurodevelopmental syndrome
GPathogenic/Likely pathogenic
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