rs10128556
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10128556(C;C) |
| Make rs10128556(C;T) |
| Make rs10128556(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5242453 |
| Gene | HBBP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10128556 |
| dbSNP (classic) | rs10128556 |
| ClinGen | rs10128556 |
| ebi | rs10128556 |
| HLI | rs10128556 |
| Exac | rs10128556 |
| Gnomad | rs10128556 |
| Varsome | rs10128556 |
| LitVar | rs10128556 |
| Map | rs10128556 |
| PheGenI | rs10128556 |
| Biobank | rs10128556 |
| 1000 genomes | rs10128556 |
| hgdp | rs10128556 |
| ensembl | rs10128556 |
| geneview | rs10128556 |
| scholar | rs10128556 |
| rs10128556 | |
| pharmgkb | rs10128556 |
| gwascentral | rs10128556 |
| openSNP | rs10128556 |
| 23andMe | rs10128556 |
| SNPshot | rs10128556 |
| SNPdbe | rs10128556 |
| MSV3d | rs10128556 |
| GWAS Ctlg | rs10128556 |
| GMAF | 0.2011 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 20353593
] Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.
[PMID 29313433] Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant.
