{{Rsnum
|rsid=11653545
|Gene=FXR2
|Chromosome=17
|position=7608756
|Orientation=plus
|GMAF=0.08448
|Gene_s=FXR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 2.7 | 97.3
| HCB | 5.2 | 35.6 | 59.3
| JPT | 7.1 | 42.5 | 50.4
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 5.2 | 35.6 | 59.3
| CHD | 3.7 | 31.2 | 65.1
| GIH | 0.0 | 8.0 | 92.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 29.8 | 70.2
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 2.0 | 98.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23118916
  |Trait=IgM levels
  |Title=Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population.
  |RiskAllele=G
  |Pval=2E-7
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}