rs976881
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs976881(A;A) |
| Make rs976881(A;G) |
| Make rs976881(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 12173697 |
| Gene | TNFRSF1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs976881 |
| dbSNP (classic) | rs976881 |
| ClinGen | rs976881 |
| ebi | rs976881 |
| HLI | rs976881 |
| Exac | rs976881 |
| Gnomad | rs976881 |
| Varsome | rs976881 |
| LitVar | rs976881 |
| Map | rs976881 |
| PheGenI | rs976881 |
| Biobank | rs976881 |
| 1000 genomes | rs976881 |
| hgdp | rs976881 |
| ensembl | rs976881 |
| geneview | rs976881 |
| scholar | rs976881 |
| rs976881 | |
| pharmgkb | rs976881 |
| gwascentral | rs976881 |
| openSNP | rs976881 |
| 23andMe | rs976881 |
| SNPshot | rs976881 |
| SNPdbe | rs976881 |
| MSV3d | rs976881 |
| GWAS Ctlg | rs976881 |
| GMAF | 0.2709 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 22860894] Genetic polymorphisms of tumour necrosis factor receptor superfamily 1b and fas ligand are associated with clinical efficacy and/or acute severe infusion reactions to infliximab in Crohn's disease
[PMID 19442614] Multiple osteoporosis susceptibility genes on chromosome 1p36 in Chinese.
[PMID 20488723] Genetic determinants of circulating levels of tumor necrosis factor receptor II and their association with TNF-RII gene polymorphisms.
