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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC121815964, NFKB2
Single nucleotide variant
(intron variant)
not specified
GBenign
LOC121815964, NFKB2
Single nucleotide variant
(intron variant)
Immunodeficiency, common variable, 10
+1 more
GBenign