C4225277[trait identifier] AND "Institute of Human Genetics, Cologne U - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1328476	NM_003998.4(NFKB1):c.1210+1G>A	NFKB1	Single nucleotide variant (splice donor variant)	Immunodeficiency, common variable, 12 +1 more	GConflicting classifications of pathogenicity
Select item 983472	NM_003998.4(NFKB1):c.2671del (p.Ala891fs)	NFKB1 (A877fs +2 more)	Deletion (frameshift variant)	Immunodeficiency, common variable, 12	GLikely pathogenic