{{Rsnum
|rsid=4985726
|Gene=TNFRSF13B
|Chromosome=17
|position=16960324
|Orientation=plus
|GMAF=0.1694
|Gene_s=TNFRSF13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 84.4 | 14.1 | 1.6
| HCB | 50.0 | 38.6 | 11.4
| JPT | 50.0 | 33.3 | 16.7
| YRI | 88.3 | 11.7 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 50.0 | 38.6 | 11.4
| 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 GWAS
|PMID=22558069
|Trait=None
|Title=Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.
|RiskAllele=G
|Pval=7E-24
|OR=0.1350
|ORtxt=None
|OA=1
}}