List of variants in gene NCF2 reported as likely pathogenic for Chronic granulomatous disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000433.4(NCF2):c.1026G>A (p.Lys342=)	rs1459123494	0.00001
NM_000433.4(NCF2):c.1438del (p.Glu480fs)	rs2102875639
NM_000433.4(NCF2):c.417del (p.Ala140fs)
NM_000433.4(NCF2):c.500G>A (p.Trp167Ter)

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