"Institute of Human Genetics, University of Goettingen"[submitter] AND - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1679519	NM_015100.4(POGZ):c.2545+2del	POGZ	Deletion (splice donor variant)	Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome	GLikely pathogenic
Select item 930505	NM_015100.4(POGZ):c.1685G>A (p.Cys562Tyr)	POGZ (C500Y +4 more)	Single nucleotide variant (missense variant)	Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome	GUncertain significance