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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688390	NM_001322934.2(NFKB2):c.145-89dup	NFKB2	Duplication (intron variant)	not specified	GBenign
Select item 2628274	NM_001322934.2(NFKB2):c.395+99A>G	NFKB2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628219	NM_001322934.2(NFKB2):c.662-27T>G	LOC121815964, NFKB2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 403232	NM_001322934.2(NFKB2):c.662-11C>T	LOC121815964, NFKB2	Single nucleotide variant (intron variant)	Immunodeficiency, common variable, 10 +1 more	GBenign
Select item 2628252	NM_001322934.2(NFKB2):c.1118-112C>G	NFKB2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 403233	NM_001322934.2(NFKB2):c.1269A>G (p.Pro423=)	LOC130004599, NFKB2	Single nucleotide variant (no sequence alteration +1 more)	Immunodeficiency, common variable, 10 +1 more	GBenign
Select item 403234	NM_001322934.2(NFKB2):c.1821A>G (p.Ala607=)	NFKB2	Single nucleotide variant (no sequence alteration +1 more)	Immunodeficiency, common variable, 10 +1 more	GBenign
Select item 2628311	NM_001322934.2(NFKB2):c.2579-42T>C	NFKB2	Single nucleotide variant (intron variant)	not specified	GBenign

ClinVar