{{Rsnum
|rsid=1063054
|Gene=NBN
|Chromosome=8
|position=89934373
|Orientation=minus
|GMAF=0.315
|Gene_s=NBN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 49.2 | 41.5 | 9.2
| HCB | 35.6 | 51.1 | 13.3
| JPT | 47.7 | 36.4 | 15.9
| YRI | 63.5 | 33.3 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 35.6 | 51.1 | 13.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24113799
|Title=Functional variants in NBS1 and cancer risk: evidence from a meta-analysis of 60 publications with 111 individual studies
}}

{{PMID Auto
|PMID=18638378
|Title=Analysis of variants in DNA damage signalling genes in bladder cancer.
|OA=1
}}

{{PMID Auto
|PMID=19276285
|Title=Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.
|OA=1
}}

{{PMID Auto
|PMID=20478923
|Title=Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers.
|OA=1
}}

{{PMID Auto
|PMID=25176580
|Title=NBN and XRCC3 genetic variants in childhood acute lymphoblastic leukaemia
}}
{{on chip | FTDNA}}