{{Rsnum
|rsid=137878529
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NCF2
|position=183574507
|Gene_s=NCF2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|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.183574507T>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000433.3:c.481A>G; 608515.0002
|Disease=Chronic granulomatous disease
|FwdALT=C
|FwdREF=T
|GENEINFO=NCF2:4688
|GENE_ID=4688
|GENE_NAME=NCF2
|REF=T
|RSPOS=183574507
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260080a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=137878529
|CLNORIGIN=1
}}