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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYBA
(W131*)
Single nucleotide variant
(nonsense)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
GPathogenic
CYBA
(G39S)
Single nucleotide variant
(missense variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
GUncertain significance