C1970859[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 10933	NM_000397.4(CYBB):c.252G>A (p.Ala84=)	CYBB	Single nucleotide variant (synonymous variant)	Granulomatous disease, chronic, X-linked +2 more	GPathogenic
Select item 643505	NM_000397.4(CYBB):c.662T>C (p.Ile221Thr)	CYBB (I221T)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1505442	NM_000397.4(CYBB):c.772C>G (p.Pro258Ala)	CYBB (P258A)	Single nucleotide variant (missense variant)	Granulomatous disease, chronic, X-linked +1 more	GUncertain significance
Select item 68372	NM_000397.4(CYBB):c.1090G>C (p.Gly364Arg)	CYBB (G364R)	Single nucleotide variant (missense variant)	Granulomatous disease, chronic, X-linked +2 more	GBenign/Likely benign
Select item 965223	NM_000397.4(CYBB):c.1291G>A (p.Ala431Thr)	CYBB (A431T)	Single nucleotide variant (missense variant)	Granulomatous disease, chronic, X-linked +1 more	GUncertain significance
Select item 732210	NM_000397.4(CYBB):c.1414G>A (p.Gly472Ser)	CYBB (G472S)	Single nucleotide variant (missense variant)	X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency +4 more	GConflicting classifications of pathogenicity

ClinVar