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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1259250	NM_000619.3(IFNG):c.366+284G>A	IFNG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282751	NM_000619.3(IFNG):c.115-4_115-3del	IFNG	Deletion (intron variant)	not provided	GBenign
Select item 402962	NM_000619.3(IFNG):c.115-3del	IFNG	Deletion (intron variant)	not specified +2 more	GBenign

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