{{Rsnum
|rsid=137854593
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CYBB
|position=37809604
|Gene_s=CYBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300481
|variant=0011
|rsnum=137854593
}}{{ClinVar
|rsid=137854593
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=37668857
|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
|CLNHGVS=NC_000023.10:g.37668857A>G
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=300481.0011; VAR_002441
|CLNSIG=5
|CLNCUI=C1844376
|CLNDBN=Chronic granulomatous disease, X-linked; not provided
|Disease=Chronic granulomatous disease; not provided
|CLNACC=RCV000011678.1; RCV000059242.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1844376:306400:379
}}{{PMID Auto
|PMID=8182143
|Title=A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox.
|OA=1
}}