rs55870409
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs55870409(C;C) |
| Make rs55870409(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 173592 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs55870409 |
| dbSNP (classic) | rs55870409 |
| ClinGen | rs55870409 |
| ebi | rs55870409 |
| HLI | rs55870409 |
| Exac | rs55870409 |
| Gnomad | rs55870409 |
| Varsome | rs55870409 |
| LitVar | rs55870409 |
| Map | rs55870409 |
| PheGenI | rs55870409 |
| Biobank | rs55870409 |
| 1000 genomes | rs55870409 |
| hgdp | rs55870409 |
| ensembl | rs55870409 |
| geneview | rs55870409 |
| scholar | rs55870409 |
| rs55870409 | |
| pharmgkb | rs55870409 |
| gwascentral | rs55870409 |
| openSNP | rs55870409 |
| 23andMe | rs55870409 |
| SNPshot | rs55870409 |
| SNPdbe | rs55870409 |
| MSV3d | rs55870409 |
| GWAS Ctlg | rs55870409 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs55870409(C;C) |
| Alt | rs55870409(C;C) |
| Reference | Rs55870409(T;T) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.223591T>C |
| CLNSRC | |
| CLNACC | |
[PMID 1390944] Hemoglobin Rouen (alpha-140 (HC2) Tyr-->His): alteration of the alpha-chain C-terminal region and moderate increase in oxygen affinity.
[PMID 1428951] Hb Ethiopia or alpha 2(140)(HC2)Tyr----His beta 2.
