rs884409
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs884409(G;G) |
| Make rs884409(G;T) |
| Make rs884409(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 171522147 |
| Gene | CYBRD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs884409 |
| dbSNP (classic) | rs884409 |
| ClinGen | rs884409 |
| ebi | rs884409 |
| HLI | rs884409 |
| Exac | rs884409 |
| Gnomad | rs884409 |
| Varsome | rs884409 |
| LitVar | rs884409 |
| Map | rs884409 |
| PheGenI | rs884409 |
| Biobank | rs884409 |
| 1000 genomes | rs884409 |
| hgdp | rs884409 |
| ensembl | rs884409 |
| geneview | rs884409 |
| scholar | rs884409 |
| rs884409 | |
| pharmgkb | rs884409 |
| gwascentral | rs884409 |
| openSNP | rs884409 |
| 23andMe | rs884409 |
| SNPshot | rs884409 |
| SNPdbe | rs884409 |
| MSV3d | rs884409 |
| GWAS Ctlg | rs884409 |
| GMAF | 0.2199 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19673882
] A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis
[PMID 22773607] CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients.
