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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYBB
(F262C)
Single nucleotide variant
(missense variant)
Granulomatous disease, chronic, X-linked
GLikely pathogenic
CYBB
Single nucleotide variant
(splice donor variant)
Granulomatous disease, chronic, X-linked
GPathogenic