C3809991[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333761	NM_001322934.2(NFKB2):c.1407C>G (p.Asp469Glu)	NFKB2 (D427E +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 10	GUncertain significance
Select item 1333762	NM_001322934.2(NFKB2):c.2657C>A (p.Pro886Gln)	NFKB2 (P844Q +2 more)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 10	GUncertain significance