rs10421768
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10421768(A;A) |
| Make rs10421768(A;G) |
| Make rs10421768(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 35281996 |
| Gene | HAMP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10421768 |
| dbSNP (classic) | rs10421768 |
| ClinGen | rs10421768 |
| ebi | rs10421768 |
| HLI | rs10421768 |
| Exac | rs10421768 |
| Gnomad | rs10421768 |
| Varsome | rs10421768 |
| LitVar | rs10421768 |
| Map | rs10421768 |
| PheGenI | rs10421768 |
| Biobank | rs10421768 |
| 1000 genomes | rs10421768 |
| hgdp | rs10421768 |
| ensembl | rs10421768 |
| geneview | rs10421768 |
| scholar | rs10421768 |
| rs10421768 | |
| pharmgkb | rs10421768 |
| gwascentral | rs10421768 |
| openSNP | rs10421768 |
| 23andMe | rs10421768 |
| SNPshot | rs10421768 |
| SNPdbe | rs10421768 |
| MSV3d | rs10421768 |
| GWAS Ctlg | rs10421768 |
| GMAF | 0.1547 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19734422
] Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major
[PMID 31936202] The Prevalence of Insomnia and the Link between Iron Metabolism Genes Polymorphisms, TF rs1049296 C>T, TF rs3811647 G>A, TFR rs7385804 A>C, HAMP rs10421768 A>G and Sleep Disorders in Polish Individuals with ASD.
