{{Rsnum
|rsid=1234313
|Gene=TNFSF4
|Chromosome=1
|position=173197108
|Orientation=plus
|GMAF=0.3825
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TNFSF4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 11.5 | 49.6 | 38.9
| HCB | 39.4 | 48.9 | 11.7
| JPT | 57.1 | 36.6 | 6.2
| YRI | 1.4 | 15.6 | 83.0
| ASW | 0.0 | 21.1 | 78.9
| CHB | 39.4 | 48.9 | 11.7
| CHD | 44.0 | 43.1 | 12.8
| GIH | 16.8 | 51.5 | 31.7
| LWK | 2.7 | 14.5 | 82.7
| MEX | 24.1 | 53.4 | 22.4
| MKK | 1.9 | 42.3 | 55.8
| TSI | 12.7 | 39.2 | 48.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21402531
|Title=[Association study between TNFSF4 and coronary heart disease]
}}

{{PMID Auto
|PMID=19357697
|Title=Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese.
|OA=1
}}

{{PMID Auto
|PMID=21244681
|Title=Thymic stromal lymphopoietin (TSLP) is associated with allergic rhinitis in children with asthma.
|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
}}

{{PMID Auto
|PMID=23622253
|Title=Association of TNFSF4 polymorphisms with susceptibility to primary Sjögren's syndrome and primary biliary cirrhosis in a Chinese Han population
}}

{{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
}}

{{PMID Auto
|PMID=22870213
|Title=Association of OX40L polymorphisms with sporadic breast cancer in northeast Chinese Han population.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}