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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFKB2
(R579H +1 more)
Single nucleotide variant
(missense variant)
NFKB2-related condition
+2 more
GConflicting classifications of pathogenicity
NFKB2
Single nucleotide variant
(synonymous variant)
Immunodeficiency, common variable, 10
GConflicting classifications of pathogenicity
NFKB2
Single nucleotide variant
(intron variant)
NFKB2-related condition
+2 more
GConflicting classifications of pathogenicity
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