{{Rsnum
|rsid=1234314
|Gene=TNFSF4
|Chromosome=1
|position=173208253
|Orientation=plus
|GMAF=0.382
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=TNFSF4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 30.8 | 53.8 | 15.4
| HCB | 37.8 | 53.3 | 8.9
| JPT | 45.5 | 43.2 | 11.4
| YRI | 57.1 | 34.9 | 7.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 37.8 | 53.3 | 8.9
| 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
|PMID=19778912
|Title=Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis
|OA=1
}}

{{PMID Auto
|PMID=21402531
|Title=[Association study between TNFSF4 and coronary heart disease]
}}

{{PMID Auto
|PMID=21187296
|Title=A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort.
}}

{{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
}}

{{PMID Auto
|PMID=23874208
|Title=Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4
|OA=1
}}

{{PMID Auto
|PMID=24595151
|Title=Absence of association between atherosclerotic cerebral infarction and TNFSF4/TNFRSF4 single nucleotide polymorphisms rs1234313, rs1234314 and rs17568 in a Chinese population
}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}