rs9366637
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs9366637(C;T) |
| Make rs9366637(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 26088870 |
| Gene | HFE, LOC108783645 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9366637 |
| dbSNP (classic) | rs9366637 |
| ClinGen | rs9366637 |
| ebi | rs9366637 |
| HLI | rs9366637 |
| Exac | rs9366637 |
| Gnomad | rs9366637 |
| Varsome | rs9366637 |
| LitVar | rs9366637 |
| Map | rs9366637 |
| PheGenI | rs9366637 |
| Biobank | rs9366637 |
| 1000 genomes | rs9366637 |
| hgdp | rs9366637 |
| ensembl | rs9366637 |
| geneview | rs9366637 |
| scholar | rs9366637 |
| rs9366637 | |
| pharmgkb | rs9366637 |
| gwascentral | rs9366637 |
| openSNP | rs9366637 |
| 23andMe | rs9366637 |
| SNPshot | rs9366637 |
| SNPdbe | rs9366637 |
| MSV3d | rs9366637 |
| GWAS Ctlg | rs9366637 |
| GMAF | 0.2259 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21696736] Plasma ferritin levels, genetic variations in HFE gene, and coronary heart disease in Chinese: A case-control study
[PMID 23792061] Meta-analyses of HFE variants in coronary heart disease
[PMID 26054392
] Natural selection on HFE in Asian populations contributes to enhanced non-heme iron absorption
