rs63750752
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| (A;G) | 3 | Alpha-thalassemia allele carrier |
| Make rs63750752(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 173482 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs63750752 |
| dbSNP (classic) | rs63750752 |
| ClinGen | rs63750752 |
| ebi | rs63750752 |
| HLI | rs63750752 |
| Exac | rs63750752 |
| Gnomad | rs63750752 |
| Varsome | rs63750752 |
| LitVar | rs63750752 |
| Map | rs63750752 |
| PheGenI | rs63750752 |
| Biobank | rs63750752 |
| 1000 genomes | rs63750752 |
| hgdp | rs63750752 |
| ensembl | rs63750752 |
| geneview | rs63750752 |
| scholar | rs63750752 |
| rs63750752 | |
| pharmgkb | rs63750752 |
| gwascentral | rs63750752 |
| openSNP | rs63750752 |
| 23andMe | rs63750752 |
| SNPshot | rs63750752 |
| SNPdbe | rs63750752 |
| MSV3d | rs63750752 |
| GWAS Ctlg | rs63750752 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs63750752(G;G) rs63750752(T;T) |
| Alt | rs63750752(G;G) rs63750752(T;T) |
| Reference | Rs63750752(A;A) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.223481A>G; NC_000016.9:g.223481A>T |
| CLNSRC | |
| CLNACC | |
[PMID 6547932] The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatography.
[PMID 16533721] Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
