{{Rsnum
|rsid=9514827
|Chromosome=13
|position=108267055
|Orientation=plus
|GMAF=0.3021
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.8 | 44.2 | 46.9
| HCB | 21.2 | 56.9 | 21.9
| JPT | 35.4 | 38.9 | 25.7
| YRI | 0.0 | 4.8 | 95.2
| ASW | 0.0 | 22.8 | 77.2
| CHB | 21.2 | 56.9 | 21.9
| CHD | 22.0 | 50.5 | 27.5
| GIH | 14.9 | 47.5 | 37.6
| LWK | 0.9 | 17.3 | 81.8
| MEX | 3.4 | 31.0 | 65.5
| MKK | 2.6 | 33.3 | 64.1
| TSI | 9.8 | 53.9 | 36.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=23845207
|Title=B-cell activating factor genetic variants in lymphomagenesis associated with primary Sjogren's syndrome
}}

{{PMID Auto
|PMID=19383901
|Title=Genetic variation in B-cell-activating factor is associated with an increased risk of developing B-cell non-Hodgkin lymphoma.
|OA=1
}}

{{PMID Auto
|PMID=19390683
|Title=Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}