{{Rsnum
|rsid=6478106
|Gene=TNFSF15
|Chromosome=9
|position=114783386
|Orientation=plus
|GMAF=0.36
|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 | 60.2 | 32.7 | 7.1
| HCB | 44.4 | 44.4 | 11.1
| JPT | 26.5 | 47.8 | 25.7
| YRI | 28.3 | 51.0 | 20.7
| ASW | 35.1 | 45.6 | 19.3
| CHB | 44.4 | 44.4 | 11.1
| CHD | 56.0 | 36.7 | 7.3
| GIH | 48.5 | 41.6 | 9.9
| LWK | 35.5 | 48.2 | 16.4
| MEX | 36.2 | 50.0 | 13.8
| MKK | 57.1 | 35.3 | 7.7
| TSI | 44.1 | 45.1 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23266558
  |Trait=Crohn's disease
  |Title=A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
  |RiskAllele=T
  |Pval=5E-46
  |OR=1.73
  |ORtxt=[1.60-1.86]
  }}

{{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}}