rs28928884
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs28928884(C;T) |
| Make rs28928884(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 177292 |
| Gene | HBA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28928884 |
| dbSNP (classic) | rs28928884 |
| ClinGen | rs28928884 |
| ebi | rs28928884 |
| HLI | rs28928884 |
| Exac | rs28928884 |
| Gnomad | rs28928884 |
| Varsome | rs28928884 |
| LitVar | rs28928884 |
| Map | rs28928884 |
| PheGenI | rs28928884 |
| Biobank | rs28928884 |
| 1000 genomes | rs28928884 |
| hgdp | rs28928884 |
| ensembl | rs28928884 |
| geneview | rs28928884 |
| scholar | rs28928884 |
| rs28928884 | |
| pharmgkb | rs28928884 |
| gwascentral | rs28928884 |
| openSNP | rs28928884 |
| 23andMe | rs28928884 |
| SNPshot | rs28928884 |
| SNPdbe | rs28928884 |
| MSV3d | rs28928884 |
| GWAS Ctlg | rs28928884 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28928884(T;T) |
| Alt | rs28928884(T;T) |
| Reference | Rs28928884(C;C) |
| Significance | Other |
| Disease | HEMOGLOBIN CHAROLLES |
| Variation | info |
| Gene | HBA1 |
| CLNDBN | HEMOGLOBIN CHAROLLES |
| Reversed | 0 |
| HGVS | NC_000016.9:g.227291C>T |
| CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000017222.2, |
[PMID 10569723] Two new alpha chain variants: Hb Boghe [alpha58(E7)His-->Gln, alpha2], a variant on the distal histidine, and Hb CHarolles [alpha103(G10)His-Tyr, alpha1].
