{{Rsnum
|rsid = 34730753
|Status = Merged
|Merged = 2274064
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=1
|position=183573252
|Gene=NCF2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NCF2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.4 | 48.7 | 31.0
| HCB | 39.4 | 50.4 | 10.2
| JPT | 48.7 | 44.2 | 7.1
| YRI | 8.2 | 46.3 | 45.6
| ASW | 10.5 | 57.9 | 31.6
| CHB | 39.4 | 50.4 | 10.2
| CHD | 33.9 | 47.7 | 18.3
| GIH | 25.7 | 54.5 | 19.8
| LWK | 10.9 | 46.4 | 42.7
| MEX | 41.4 | 44.8 | 13.8
| MKK | 9.6 | 39.1 | 51.3
| TSI | 20.6 | 48.0 | 31.4
| HapMapRevision=28
}}{{Venter SNP
|rsid=34730753
|allele=C
|frequency=
|uid=1103675279655
|type=homozygous_SNP
|hugo=NCF2
|ensembl gene=ENSG00000116701
|ensembl transcript=ENST00000367535
|sift=TOLERATED
|disease=Defects in NCF2 are a cause of autosomal recessive chronic granulomatous disease (AR-CGD) (MIM:233710); also known as autosomal cytochrome-b-positive chronic granulomatous disease. It causes recurrent infection by catalase-positive organisms.
}}