rs1061624
| Orientation | plus |
| Stabilized | plus |
| Make rs1061624(A;A) |
| Make rs1061624(A;G) |
| Make rs1061624(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 12207208 |
| Gene | TNFRSF1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1061624 |
| dbSNP (classic) | rs1061624 |
| ClinGen | rs1061624 |
| ebi | rs1061624 |
| HLI | rs1061624 |
| Exac | rs1061624 |
| Gnomad | rs1061624 |
| Varsome | rs1061624 |
| LitVar | rs1061624 |
| Map | rs1061624 |
| PheGenI | rs1061624 |
| Biobank | rs1061624 |
| 1000 genomes | rs1061624 |
| hgdp | rs1061624 |
| ensembl | rs1061624 |
| geneview | rs1061624 |
| scholar | rs1061624 |
| rs1061624 | |
| pharmgkb | rs1061624 |
| gwascentral | rs1061624 |
| openSNP | rs1061624 |
| 23andMe | rs1061624 |
| SNPshot | rs1061624 |
| SNPdbe | rs1061624 |
| MSV3d | rs1061624 |
| GWAS Ctlg | rs1061624 |
| GMAF | 0.4688 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 19421420
] Tumor Necrosis Factor Receptor Superfamily, Member 1B Haplotypes Increase or Decrease the Risk of Inflammatory Bowel Diseases in a New Zealand Caucasian Population
[PMID 21995493] TNFRSF1B +676 T>G polymorphism predicts survival of non-Small cell lung cancer patients treated with chemoradiotherapy
[PMID 17705862] Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples.
[PMID 18248655] Genetic polymorphisms of tumour necrosis factor receptor superfamily 1A and 1B affect responses to infliximab in Japanese patients with Crohn's disease.
[PMID 18603647] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
[PMID 19390683] Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk.
[PMID 20007930] A functional haplotype in the 3'untranslated region of TNFRSF1B is associated with tuberculosis in two African populations.
[PMID 20646319] 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.
[PMID 21554999] Polymorphism of 3'UTR region of TNFR2 coding gene and its role in clinical tuberculosis in Han Chinese pediatric population.
[PMID 25010932] Association of TNF-α, TNFRSF1A and TNFRSF1B Gene Polymorphisms with the Risk of Sporadic Breast Cancer in Northeast Chinese Han Women
[PMID 30254506] Polymorphic Variants of TNFR2 Gene in Schizophrenia and Its Interaction with -308G/A TNF-α Gene Polymorphism.
