rs2718812
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2718812(A;A) |
| Make rs2718812(A;G) |
| Make rs2718812(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 133680858 |
| Gene | TF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2718812 |
| dbSNP (classic) | rs2718812 |
| ClinGen | rs2718812 |
| ebi | rs2718812 |
| HLI | rs2718812 |
| Exac | rs2718812 |
| Gnomad | rs2718812 |
| Varsome | rs2718812 |
| LitVar | rs2718812 |
| Map | rs2718812 |
| PheGenI | rs2718812 |
| Biobank | rs2718812 |
| 1000 genomes | rs2718812 |
| hgdp | rs2718812 |
| ensembl | rs2718812 |
| geneview | rs2718812 |
| scholar | rs2718812 |
| rs2718812 | |
| pharmgkb | rs2718812 |
| gwascentral | rs2718812 |
| openSNP | rs2718812 |
| 23andMe | rs2718812 |
| SNPshot | rs2718812 |
| SNPdbe | rs2718812 |
| MSV3d | rs2718812 |
| GWAS Ctlg | rs2718812 |
| GMAF | 0.4807 |
| 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 | 0.000001 |
| Odds Ratio | NR NR |
