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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFKB2
(Q413fs +1 more)
Duplication
(frameshift variant)
Immunodeficiency, common variable, 10
GLikely pathogenic
NFKB2
(A546P +1 more)
Single nucleotide variant
(missense variant)
Immunodeficiency, common variable, 10
GUncertain significance