rs17270561
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17270561(A;A) |
| Make rs17270561(A;C) |
| Make rs17270561(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 25820211 |
| Gene | SLC17A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17270561 |
| dbSNP (classic) | rs17270561 |
| ClinGen | rs17270561 |
| ebi | rs17270561 |
| HLI | rs17270561 |
| Exac | rs17270561 |
| Gnomad | rs17270561 |
| Varsome | rs17270561 |
| LitVar | rs17270561 |
| Map | rs17270561 |
| PheGenI | rs17270561 |
| Biobank | rs17270561 |
| 1000 genomes | rs17270561 |
| hgdp | rs17270561 |
| ensembl | rs17270561 |
| geneview | rs17270561 |
| scholar | rs17270561 |
| rs17270561 | |
| pharmgkb | rs17270561 |
| gwascentral | rs17270561 |
| openSNP | rs17270561 |
| 23andMe | rs17270561 |
| SNPshot | rs17270561 |
| SNPdbe | rs17270561 |
| MSV3d | rs17270561 |
| GWAS Ctlg | rs17270561 |
| GMAF | 0.1552 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 5E-7 |
| Odds Ratio | NR NR |
