{{Rsnum
|rsid=119103276
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NCF2
|position=183577667
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NCF2
}}{{omim
|id=608515
|rsnum=119103276
|variant=0009
}}{{ClinVar
|rsid=119103276
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=183577667
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=NCF2:4688
|GENE_NAME=NCF2
|GENE_ID=4688
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.183577667G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000433.3:c.298C>T; 608515.0009
|CLNSIG=5
|CLNCUI=C1856245
|CLNDBN=Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2
|Disease=Chronic granulomatous disease
|CLNACC=RCV000002332.1
|Tags=RV;PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1856245:233710:ORPHA379
}}