List of variants reported as likely benign for Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 by Illumina Laboratory Services, Illumina

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000433.4(NCF2):c.1256A>T (p.Asn419Ile)	rs35012521	0.00520
NM_000433.4(NCF2):c.1360C>T (p.Pro454Ser)	rs55761650	0.00401
NM_000433.4(NCF2):c.563G>A (p.Arg188Lys)	rs115365142	0.00260
NM_000433.4(NCF2):c.1552G>C (p.Asp518His)	rs143901397	0.00151
NM_000433.4(NCF2):c.1183C>T (p.Arg395Trp)	rs13306575

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