{{Rsnum
|rsid=267606912
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=NCF2
|position=183574509
|Gene_s=NCF2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000002328.1
|CLNALLE=1
|CLNDBN=Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1856245:233710:ORPHA379
|CLNHGVS=NC_000001.11:g.183574509T>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000433.3:c.479A>T; NM_001190789.1:c.366+3090A>T; 608515.0002
|Disease=Chronic granulomatous disease
|FwdALT=T
|FwdREF=A
|GENEINFO=NCF2:4688
|GENE_ID=4688
|GENE_NAME=NCF2
|REF=T
|RSPOS=183574509
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260080a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267606912
|CLNORIGIN=1
}}