{{Rsnum
|rsid=3397
|Gene=TNFRSF1B
|Chromosome=1
|position=12207235
|Orientation=plus
|GMAF=0.4486
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TNFRSF1B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 17.5 | 61.9 | 20.6
| HCB | 46.7 | 31.1 | 22.2
| JPT | 43.2 | 40.9 | 15.9
| YRI | 77.4 | 21.0 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 46.7 | 31.1 | 22.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 20.8 | 56.2 | 22.9
| LWK | 0.0 | 0.0 | 0.0
| MEX | 8.9 | 32.1 | 58.9
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19343543
|Title=Association analysis of TNFRSF1B polymorphisms with type 2 diabetes and its related traits in North India.
|OA=1
}}

{{PMID Auto
|PMID=19421420
|Title=Tumor Necrosis Factor Receptor Superfamily, Member 1B Haplotypes Increase or Decrease the Risk of Inflammatory Bowel Diseases in a New Zealand Caucasian Population
|OA=1
}}

{{PMID Auto
|PMID=17705862
|Title=Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples.
|OA=1
}}

{{PMID Auto
|PMID=18248655
|Title=Genetic polymorphisms of tumour necrosis factor receptor superfamily 1A and 1B affect responses to infliximab in Japanese patients with Crohn's disease.
}}

{{PMID Auto
|PMID=18603647
|Title=Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
|OA=1
}}

{{PMID Auto
|PMID=20007930
|Title=A functional haplotype in the 3'untranslated region of TNFRSF1B is associated with tuberculosis in two African populations.
|OA=1
}}

{{PMID Auto
|PMID=20646319
|Title=TNFRSF1B A1466G genotype is predictive of clinical efficacy after treatment with a definitive 5-fluorouracil/cisplatin-based chemoradiotherapy in Japanese patients with esophageal squamous cell carcinoma.
|OA=1
}}

{{PMID Auto
|PMID=21554999
|Title=Polymorphism of 3'UTR region of TNFR2 coding gene and its role in clinical tuberculosis in Han Chinese pediatric population.
}}

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