{{Rsnum
|rsid=10912564
|Gene=TNFSF4
|Chromosome=1
|position=173201479
|Orientation=plus
|GMAF=0.3416
|Gene_s=TNFSF4
|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 | 43.9 | 46.7 | 9.3
| HCB | 77.8 | 22.2 | 0.0
| JPT | 88.9 | 11.1 | 0.0
| YRI | 7.7 | 35.9 | 56.3
| ASW | 5.4 | 51.8 | 42.9
| CHB | 77.8 | 22.2 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 10.0 | 44.5 | 45.5
| MEX | 0.0 | 0.0 | 0.0
| MKK | 15.8 | 52.0 | 32.2
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22536368
|Title=CD3Z Genetic Polymorphism in Immune Response to Hepatitis B Vaccination in Two Independent Chinese Populations
|OA=1
}}

{{PMID Auto
|PMID=21445270
|Title=A common polymorphism in the promoter region of the TNFSF4 gene is associated with lower allele-specific expression and risk of myocardial infarction.
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}