rs1224141
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1224141(G;G) |
| Make rs1224141(G;T) |
| Make rs1224141(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 108283375 |
| Gene | TNFSF13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1224141 |
| dbSNP (classic) | rs1224141 |
| ClinGen | rs1224141 |
| ebi | rs1224141 |
| HLI | rs1224141 |
| Exac | rs1224141 |
| Gnomad | rs1224141 |
| Varsome | rs1224141 |
| LitVar | rs1224141 |
| Map | rs1224141 |
| PheGenI | rs1224141 |
| Biobank | rs1224141 |
| 1000 genomes | rs1224141 |
| hgdp | rs1224141 |
| ensembl | rs1224141 |
| geneview | rs1224141 |
| scholar | rs1224141 |
| rs1224141 | |
| pharmgkb | rs1224141 |
| gwascentral | rs1224141 |
| openSNP | rs1224141 |
| 23andMe | rs1224141 |
| SNPshot | rs1224141 |
| SNPdbe | rs1224141 |
| MSV3d | rs1224141 |
| GWAS Ctlg | rs1224141 |
| GMAF | 0.1511 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23845207] B-cell activating factor genetic variants in lymphomagenesis associated with primary Sjogren's syndrome
[PMID 19051265
] Serum BLyS levels increase after rituximab as initial therapy in patients with follicular Grade 1 non-Hodgkin lymphoma.
[PMID 19383901] Genetic variation in B-cell-activating factor is associated with an increased risk of developing B-cell non-Hodgkin lymphoma.
