"HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Isma - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1684584	NM_001289125.3(IFNAR2):c.-83-4640G>A	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (intron variant)	Mortality risk in patients with severe coronavirus disease (COVID-19) +1 more	GUncertain significance; association
Select item 7288	NM_001289125.3(IFNAR2):c.23T>C (p.Phe8Ser)	IFNAR2, IFNAR2-IL10RB (F8S)	Single nucleotide variant (missense variant)	Immunodeficiency 45 +2 more	GBenign
Select item 2628357	NM_001289125.3(IFNAR2):c.28T>A (p.Phe10Ile)	IFNAR2-IL10RB, IFNAR2 (F10I)	Single nucleotide variant (missense variant)	Associated with severe COVID-19 disease	GUncertain significance
Select item 1170800	NM_001289125.3(IFNAR2):c.28T>G (p.Phe10Val)	IFNAR2, IFNAR2-IL10RB (F10V)	Single nucleotide variant (missense variant)	Immunodeficiency 45 +2 more	GBenign
Select item 2628358	NM_001289125.3(IFNAR2):c.98-43T>A	IFNAR2-IL10RB, IFNAR2	Single nucleotide variant (intron variant)	Associated with severe COVID-19 disease	GUncertain significance
Select item 1684582	NM_001289125.3(IFNAR2):c.98-43T>C	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1684583	NM_001289125.3(IFNAR2):c.541-50A>G	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

ClinVar