rs9514827
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9514827(C;C) |
| Make rs9514827(C;T) |
| Make rs9514827(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 108267055 |
| Gene | TNFSF13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9514827 |
| dbSNP (classic) | rs9514827 |
| ClinGen | rs9514827 |
| ebi | rs9514827 |
| HLI | rs9514827 |
| Exac | rs9514827 |
| Gnomad | rs9514827 |
| Varsome | rs9514827 |
| LitVar | rs9514827 |
| Map | rs9514827 |
| PheGenI | rs9514827 |
| Biobank | rs9514827 |
| 1000 genomes | rs9514827 |
| hgdp | rs9514827 |
| ensembl | rs9514827 |
| geneview | rs9514827 |
| scholar | rs9514827 |
| rs9514827 | |
| pharmgkb | rs9514827 |
| gwascentral | rs9514827 |
| openSNP | rs9514827 |
| 23andMe | rs9514827 |
| SNPshot | rs9514827 |
| SNPdbe | rs9514827 |
| MSV3d | rs9514827 |
| GWAS Ctlg | rs9514827 |
| GMAF | 0.3021 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23845207] B-cell activating factor genetic variants in lymphomagenesis associated with primary Sjogren's syndrome
[PMID 19383901
] Genetic variation in B-cell-activating factor is associated with an increased risk of developing B-cell non-Hodgkin lymphoma.
[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.
