{{Rsnum
|rsid=137854586
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CYBB
|position=37805020
|Gene_s=CYBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300481
|variant=0002
|rsnum=137854586
}}{{ClinVar
|rsid=137854586
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=37664273
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=CYBB:1536
|GENE_NAME=CYBB
|GENE_ID=1536
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.37664273G>A; NC_000023.10:g.37664273G>C
|CLNORIGIN=1
|CLNSRCID=
VAR_025621; 300481.0002; VAR_002439
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000059231.1; RCV000011668.8; RCV000059232.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=not provided; Granulomatous disease, chronic, X-linked, variant
|CLNDSDB=MedGen
|CLNDSDBID=C1844378
|CLNSRC=UniProtKB (variants); OMIM Allelic Variant
|Disease=not provided; Granulomatous disease
}}{{PMID Auto
|PMID=1710153
|Title=Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease.
}}

{{PMID Auto
|PMID=10914676
|Title=Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiency.
}}