"Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan"[submitte - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 402970	NM_001289125.3(IFNAR2):c.841-220G>A	IFNAR2, IFNAR2-IL10RB +1 more (A285T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign
Select item 2628110	NM_000628.5(IL10RB):c.49+40G>A	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 16923	NM_000628.5(IL10RB):c.139A>G (p.Lys47Glu)	IFNAR2-IL10RB, IL10RB (K47E)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 2628197	NM_000628.5(IL10RB):c.331+65G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628185	NM_000628.5(IL10RB):c.805-2113A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628202	NM_000628.5(IL10RB):c.805-2099G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 339698	NM_000628.5(IL10RB):c.*85A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25 +2 more	GBenign
Select item 2688402	NM_001405849.1(IL10RB):c.805-886C>A	IL10RB	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688494	NM_001405849.1(IL10RB):c.805-591T>G	IL10RB	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GBenign

ClinVar