rs4792800
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4792800(A;A) |
| Make rs4792800(A;G) |
| Make rs4792800(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 16941853 |
| Gene | TNFRSF13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4792800 |
| dbSNP (classic) | rs4792800 |
| ClinGen | rs4792800 |
| ebi | rs4792800 |
| HLI | rs4792800 |
| Exac | rs4792800 |
| Gnomad | rs4792800 |
| Varsome | rs4792800 |
| LitVar | rs4792800 |
| Map | rs4792800 |
| PheGenI | rs4792800 |
| Biobank | rs4792800 |
| 1000 genomes | rs4792800 |
| hgdp | rs4792800 |
| ensembl | rs4792800 |
| geneview | rs4792800 |
| scholar | rs4792800 |
| rs4792800 | |
| pharmgkb | rs4792800 |
| gwascentral | rs4792800 |
| openSNP | rs4792800 |
| 23andMe | rs4792800 |
| SNPshot | rs4792800 |
| SNPdbe | rs4792800 |
| MSV3d | rs4792800 |
| GWAS Ctlg | rs4792800 |
| GMAF | 0.1841 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22673310] |
| Trait | |
| Title | Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population. |
| Risk Allele | G |
| P-val | 1E-12 |
| Odds Ratio | None None |
