rs8177178
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8177178(A;A) |
| Make rs8177178(A;G) |
| Make rs8177178(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 133744428 |
| Gene | TF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8177178 |
| dbSNP (classic) | rs8177178 |
| ClinGen | rs8177178 |
| ebi | rs8177178 |
| HLI | rs8177178 |
| Exac | rs8177178 |
| Gnomad | rs8177178 |
| Varsome | rs8177178 |
| LitVar | rs8177178 |
| Map | rs8177178 |
| PheGenI | rs8177178 |
| Biobank | rs8177178 |
| 1000 genomes | rs8177178 |
| hgdp | rs8177178 |
| ensembl | rs8177178 |
| geneview | rs8177178 |
| scholar | rs8177178 |
| rs8177178 | |
| pharmgkb | rs8177178 |
| gwascentral | rs8177178 |
| openSNP | rs8177178 |
| 23andMe | rs8177178 |
| SNPshot | rs8177178 |
| SNPdbe | rs8177178 |
| MSV3d | rs8177178 |
| GWAS Ctlg | rs8177178 |
| GMAF | 0.3595 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 23089144] An association of transferrin gene polymorphism and serum transferrin levels with age-related macular degeneration
[PMID 19673882
] A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.
