rs13194491
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs13194491(C;T) |
| Make rs13194491(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 27069301 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13194491 |
| dbSNP (classic) | rs13194491 |
| ClinGen | rs13194491 |
| ebi | rs13194491 |
| HLI | rs13194491 |
| Exac | rs13194491 |
| Gnomad | rs13194491 |
| Varsome | rs13194491 |
| LitVar | rs13194491 |
| Map | rs13194491 |
| PheGenI | rs13194491 |
| Biobank | rs13194491 |
| 1000 genomes | rs13194491 |
| hgdp | rs13194491 |
| ensembl | rs13194491 |
| geneview | rs13194491 |
| scholar | rs13194491 |
| rs13194491 | |
| pharmgkb | rs13194491 |
| gwascentral | rs13194491 |
| openSNP | rs13194491 |
| 23andMe | rs13194491 |
| SNPshot | rs13194491 |
| SNPdbe | rs13194491 |
| MSV3d | rs13194491 |
| GWAS Ctlg | rs13194491 |
| GMAF | 0.03076 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 1E-8 |
| Odds Ratio | NR NR |
[PMID 26460247] Genetic contribution to iron status: SNPs related to iron deficiency anaemia and fine mapping of CACNA2D3 calcium channel subunit
