{{Rsnum
|rsid=13306575
|Gene=NCF2
|Chromosome=1
|position=183563302
|Orientation=plus
|GMAF=0.01653
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NCF2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 98.2 | 1.8 | 0.0
| HCB | 89.6 | 10.4 | 0.0
| JPT | 93.6 | 5.5 | 0.9
| YRI | 99.3 | 0.7 | 0.0
| ASW | 94.7 | 5.3 | 0.0
| CHB | 89.6 | 10.4 | 0.0
| CHD | 89.9 | 10.1 | 0.0
| GIH | 98.0 | 2.0 | 0.0
| LWK | 97.2 | 2.8 | 0.0
| MEX | 80.7 | 19.3 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 99.0 | 1.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=608515
|rsnum=13306575
|variant=0010
}}

{{ClinVar
|rsid=13306575
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=183563302
|CHROM=1
|GMAF=0.0165
|dbSNPBuildID=121
|SSR=0
|SAO=1
|VP=0x050168000b15150517110110
|GENEINFO=NCF2:4688
|GENE_NAME=NCF2
|GENE_ID=4688
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.183563302G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000433.3:c.1183C>T; 608515.0010
|CLNSIG=5
|CLNCUI=C1856245
|CLNDBN=Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2
|Disease=Chronic granulomatous disease
|CLNACC=RCV000002336.1
|Tags=RV;PM;PMC;SLO;NSM;REF;SYN;OTH;ASP;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM;NOC
|CAF=0.9835; 0.01653
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1856245:233710:ORPHA379
|COMMON=1
}}

{{PMID Auto
|PMID=16608528
|Title=Genetic polymorphisms and susceptibility to lung disease.
|OA=1
}}

{{PMID Auto
|PMID=17897462
|Title=A case-control study of rheumatoid arthritis identifies an associated single nucleotide polymorphism in the NCF4 gene, supporting a role for the NADPH-oxidase complex in autoimmunity.
|OA=1
}}

{{GET Evidence
|gene=NCF2
|aa_change=Arg395Trp
|aa_change_short=R395W
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs13306575
|overall_frequency_n=11
|overall_frequency_d=10758
|overall_frequency=0.00102249
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|in_omim=Y
|pph2_score=0.989
|genetests_testable=Y
|nblosum100=7
|autoscore=5
|webscore=N
|n_web_uneval=10
}}

{{PMID Auto
|PMID=24163247
|Title=Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}