rs4985726
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4985726(C;C) |
| Make rs4985726(C;G) |
| Make rs4985726(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 16960324 |
| Gene | TNFRSF13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4985726 |
| dbSNP (classic) | rs4985726 |
| ClinGen | rs4985726 |
| ebi | rs4985726 |
| HLI | rs4985726 |
| Exac | rs4985726 |
| Gnomad | rs4985726 |
| Varsome | rs4985726 |
| LitVar | rs4985726 |
| Map | rs4985726 |
| PheGenI | rs4985726 |
| Biobank | rs4985726 |
| 1000 genomes | rs4985726 |
| hgdp | rs4985726 |
| ensembl | rs4985726 |
| geneview | rs4985726 |
| scholar | rs4985726 |
| rs4985726 | |
| pharmgkb | rs4985726 |
| gwascentral | rs4985726 |
| openSNP | rs4985726 |
| 23andMe | rs4985726 |
| SNPshot | rs4985726 |
| SNPdbe | rs4985726 |
| MSV3d | rs4985726 |
| GWAS Ctlg | rs4985726 |
| GMAF | 0.1694 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22558069 ]
|
| Trait | |
| Title | Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. |
| Risk Allele | G |
| P-val | 7E-24 |
| Odds Ratio | 0.1350 None |
