{{Rsnum
|rsid = 119103275
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NCF2
|position=183586922
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NCF2
}}{{omim
|id=608515
|rsnum=119103275
|variant=0008
}}
{{omim
|id=233710
|rsnum=119103275
}}{{ClinVar
|rsid=119103275
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=183586922
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000a05000002110100
|GENEINFO=NCF2:4688
|GENE_NAME=NCF2
|GENE_ID=4688
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.183586922C>T
|CLNSRC=ClinVar; OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=NM_000433.3:c.230G>A; 608515.0008; VAR_017388
|CLNSIG=5
|CLNCUI=C1856245
|CLNDBN=Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2
|Disease=Chronic granulomatous disease
|CLNACC=RCV000002335.2
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1856245:233710:ORPHA379
}}{{PMID Auto
|PMID=10598813
|Title=Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase.
}}