Related gene-specific medical variations for Gene (Select 3458) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1331006	NM_000619.3(IFNG):c.409A>G (p.Ile137Val)	IFNG (I137V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 111229	NM_000619.3(IFNG):c.367-419T>C	IFNG	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 111228	NM_000619.3(IFNG):c.367-282T>A	IFNG	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 111227	NM_000619.3(IFNG):c.367-227G>C	IFNG	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 111226	NM_000619.3(IFNG):c.366+360G>C	IFNG	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 111225	NM_000619.3(IFNG):c.366+350A>T	IFNG	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 111224	NM_000619.3(IFNG):c.366+139T>C	IFNG	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 111223	NM_000619.3(IFNG):c.115-156A>G	IFNG	Single nucleotide variant (intron variant)	not provided	Gnot provided

ClinVar