"Daryl Scott Lab, Baylor College of Medicine"[submitter] AND "FOXP1"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 987888	NM_001349338.3(FOXP1):c.1718_1722+8del	FOXP1	Deletion (splice donor variant)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GPathogenic
Select item 1064533	Single allele	EIF4E3, EOGT +12 more	Deletion	See cases	GPathogenic