"GeneDx"[submitter] AND "IRF2BP1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1315569	NM_015649.3(IRF2BP1):c.1689C>T (p.Phe563=)	IRF2BP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1315568	NM_015649.3(IRF2BP1):c.1530A>G (p.Leu510=)	IRF2BP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 253540	GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1	APOC1, APOC2 +120 more	Copy number loss	See cases	GPathogenic

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