"Human Evolutionary Genetics, Institut Pasteur"[submitter] AND "IFNG"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 111222	NM_000619.3(IFNG):c.*93TCAA[1]	IFNG	Microsatellite (3 prime UTR variant)	not provided +1 more	GUncertain significance
Select item 111227	NM_000619.3(IFNG):c.367-227G>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 111229	NM_000619.3(IFNG):c.367-419T>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