rs1041569
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1041569(A;A) |
| Make rs1041569(A;T) |
| Make rs1041569(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 108267195 |
| Gene | TNFSF13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1041569 |
| dbSNP (classic) | rs1041569 |
| ClinGen | rs1041569 |
| ebi | rs1041569 |
| HLI | rs1041569 |
| Exac | rs1041569 |
| Gnomad | rs1041569 |
| Varsome | rs1041569 |
| LitVar | rs1041569 |
| Map | rs1041569 |
| PheGenI | rs1041569 |
| Biobank | rs1041569 |
| 1000 genomes | rs1041569 |
| hgdp | rs1041569 |
| ensembl | rs1041569 |
| geneview | rs1041569 |
| scholar | rs1041569 |
| rs1041569 | |
| pharmgkb | rs1041569 |
| gwascentral | rs1041569 |
| openSNP | rs1041569 |
| 23andMe | rs1041569 |
| SNPshot | rs1041569 |
| SNPdbe | rs1041569 |
| MSV3d | rs1041569 |
| GWAS Ctlg | rs1041569 |
| GMAF | 0.1556 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23845207] B-cell activating factor genetic variants in lymphomagenesis associated with primary Sjogren's syndrome
[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.
