C5231482[trait identifier] AND "Rady Children's Institute for Genomic - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 985139	NM_001320.7(CSNK2B):c.72+1G>A	CSNK2B	Single nucleotide variant (splice donor variant)	Inborn genetic diseases +1 more	GPathogenic/Likely pathogenic
Select item 1301884	NM_001320.7(CSNK2B):c.367+1G>A	CSNK2B	Single nucleotide variant (splice donor variant)	Poirier-Bienvenu neurodevelopmental syndrome	GPathogenic