{{Rsnum
|rsid=4273077
|Gene=TNFRSF13B
|Chromosome=17
|position=16945825
|Orientation=plus
|GMAF=0.2176
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TNFRSF13B
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 78.6 | 20.5 | 0.9
| HCB | 31.3 | 50.0 | 18.7
| JPT | 27.9 | 49.5 | 22.5
| YRI | 69.4 | 28.6 | 2.0
| ASW | 77.2 | 19.3 | 3.5
| CHB | 31.3 | 50.0 | 18.7
| CHD | 22.4 | 56.1 | 21.5
| GIH | 66.3 | 32.7 | 1.0
| LWK | 78.9 | 18.3 | 2.8
| MEX | 66.7 | 31.6 | 1.8
| MKK | 77.6 | 21.2 | 1.3
| TSI | 78.2 | 20.8 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20139978
|Trait=Hematological and biochemical traits
|Title=Genome-wide association study of hematological and biochemical traits in a Japanese population
|RiskAllele=G
|Pval=3E-10
|OR=0.38
|ORtxt=[NR] % variance
}}

{{PMID Auto
|PMID=24449210
|Title=Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}