{{Rsnum
|rsid=137854594
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CYBB
|position=37792023
|Gene_s=CYBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300481
|variant=0012
|rsnum=137854594
}}{{ClinVar
|rsid=137854594
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=37651276
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=CYBB:1536
|GENE_NAME=CYBB
|GENE_ID=1536
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.37651276C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000011679.4; RCV000059256.1
|CLNDBN=Granulomatous disease, chronic, X-linked, variant; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C1844378
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=300481.0012; VAR_007876
|Disease=Granulomatous disease; not provided
}}{{PMID|9856476}} A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous disease.

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