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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1265871	NM_003998.4(NFKB1):c.836-199G>C	NFKB1	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1170076	NM_003998.4(NFKB1):c.1143T>C (p.Ala381=)	NFKB1	Single nucleotide variant (synonymous variant)	Immunodeficiency, common variable, 12 +2 more	GBenign
Select item 1168266	NM_003998.4(NFKB1):c.1210+16T>C	NFKB1	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1256826	NM_003998.4(NFKB1):c.2592+58T>A	NFKB1	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1228617	NM_003998.4(NFKB1):c.2593-22C>G	NFKB1	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1225916	NM_003998.4(NFKB1):c.2750-149C>T	NFKB1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar