{{Rsnum
|rsid=104894514
|Gene=CYBA
|Chromosome=16
|position=88646131
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CYBA
}}{{omim
|id=608508
|rsnum=104894514
|variant=0004
}}{{ClinVar
|rsid=104894514
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=88712539
|CHROM=16
|GMAF=0.0009
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000016110100
|GENEINFO=CYBA:1535
|GENE_NAME=CYBA
|GENE_ID=1535
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000016.9:g.88712539G>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=608508.0004; VAR_005125
|CLNSIG=5
|CLNCUI=C1856255
|CLNDBN=Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative; not provided
|Disease=Granulomatous disease; not provided
|CLNACC=RCV000002347.1; RCV000059045.1
|Tags=RV;PM;PMC;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183; .
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1856255:233690:379
|COMMON=0
}}{{PMID|10910929}} Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox).