{{Rsnum
|rsid=3810936
|Gene=TNFSF15
|Chromosome=9
|position=114790605
|Orientation=plus
|ReferenceAllele=A
|GMAF=0.3058
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|effect1=
|effect2=
|effect3=
|Gene_s=TNFSF15
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 42.5 | 43.4 | 14.2
| HCB | 23.5 | 57.4 | 19.1
| JPT | 39.8 | 47.8 | 12.4
| YRI | 89.1 | 10.9 | 0.0
| ASW | 66.1 | 28.6 | 5.4
| CHB | 23.5 | 57.4 | 19.1
| CHD | 24.8 | 48.6 | 26.6
| GIH | 59.4 | 31.7 | 8.9
| LWK | 82.7 | 17.3 | 0.0
| MEX | 49.1 | 42.1 | 8.8
| MKK | 69.2 | 29.5 | 1.3
| TSI | 50.0 | 37.3 | 12.7
| HapMapRevision=28
}}Associated with increased risk for [[Crohn's disease]] in a study of 380 Korean patients.{{PMID|18422820}}

{{omim
|desc=INFLAMMATORY BOWEL DISEASE 16; IBD16
|id=612259
|rsnum=3810936
}}

{{PMID Auto GWAS
|PMID=21102463
|Trait=None
|Title=Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
|RiskAllele=C
|Pval=1E-15
|OR=1.2100
|ORtxt=[1.15-1.27]
|OA=1
}}

{{PMID Auto
|PMID=17663424
|Title=TNFSF15 is an ethnic-specific IBD gene.
|OA=1
}}

{{PMID Auto
|PMID=19262684
|Title=IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein.
|OA=1
}}

{{PMID Auto
|PMID=23388546
|Title=Association study of 71 European Crohn's disease susceptibility loci in a Japanese population
}}

{{PMID Auto
|PMID=24269700
|Title=Genetic risk and protective factors of TNFSF15 gene variants detected using single nucleotide polymorphisms in Hungarians with psoriasis and psoriatic arthritis
}}

{{PMID Auto
|PMID=25028192
|Title=Associations between TNFSF15 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: A meta-analysis
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}