rs1867504
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1867504(A;A) |
| Make rs1867504(A;G) |
| Make rs1867504(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 133691817 |
| Gene | TF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1867504 |
| dbSNP (classic) | rs1867504 |
| ClinGen | rs1867504 |
| ebi | rs1867504 |
| HLI | rs1867504 |
| Exac | rs1867504 |
| Gnomad | rs1867504 |
| Varsome | rs1867504 |
| LitVar | rs1867504 |
| Map | rs1867504 |
| PheGenI | rs1867504 |
| Biobank | rs1867504 |
| 1000 genomes | rs1867504 |
| hgdp | rs1867504 |
| ensembl | rs1867504 |
| geneview | rs1867504 |
| scholar | rs1867504 |
| rs1867504 | |
| pharmgkb | rs1867504 |
| gwascentral | rs1867504 |
| openSNP | rs1867504 |
| 23andMe | rs1867504 |
| SNPshot | rs1867504 |
| SNPdbe | rs1867504 |
| MSV3d | rs1867504 |
| GWAS Ctlg | rs1867504 |
| GMAF | 0.4187 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19084217 ]
|
| Trait | Serum markers of iron status |
| Title | Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | NR NR |
