rs11552708
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11552708(A;A) |
| Make rs11552708(A;G) |
| Make rs11552708(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 7559238 |
| Gene | TNFSF12-TNFSF13, TNFSF13 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11552708 |
| dbSNP (classic) | rs11552708 |
| ClinGen | rs11552708 |
| ebi | rs11552708 |
| HLI | rs11552708 |
| Exac | rs11552708 |
| Gnomad | rs11552708 |
| Varsome | rs11552708 |
| LitVar | rs11552708 |
| Map | rs11552708 |
| PheGenI | rs11552708 |
| Biobank | rs11552708 |
| 1000 genomes | rs11552708 |
| hgdp | rs11552708 |
| ensembl | rs11552708 |
| geneview | rs11552708 |
| scholar | rs11552708 |
| rs11552708 | |
| pharmgkb | rs11552708 |
| gwascentral | rs11552708 |
| openSNP | rs11552708 |
| 23andMe | rs11552708 |
| SNPshot | rs11552708 |
| SNPdbe | rs11552708 |
| MSV3d | rs11552708 |
| GWAS Ctlg | rs11552708 |
| GMAF | 0.1731 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23118916
] Genome-Wide Scan Identifies Variant in TNFSF13 Associated with Serum IgM in a Healthy Chinese Male Population
[PMID 17569747] APRIL polymorphism and systemic lupus erythematosus (SLE) susceptibility.
[PMID 18254984] Screening of functional and positional candidate genes in families with common variable immunodeficiency.
[PMID 22136669] Angiogenesis-related gene expression analysis in celiac disease.
