rs56348461
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs56348461(A;C) |
| Make rs56348461(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 173590 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs56348461 |
| dbSNP (classic) | rs56348461 |
| ClinGen | rs56348461 |
| ebi | rs56348461 |
| HLI | rs56348461 |
| Exac | rs56348461 |
| Gnomad | rs56348461 |
| Varsome | rs56348461 |
| LitVar | rs56348461 |
| Map | rs56348461 |
| PheGenI | rs56348461 |
| Biobank | rs56348461 |
| 1000 genomes | rs56348461 |
| hgdp | rs56348461 |
| ensembl | rs56348461 |
| geneview | rs56348461 |
| scholar | rs56348461 |
| rs56348461 | |
| pharmgkb | rs56348461 |
| gwascentral | rs56348461 |
| openSNP | rs56348461 |
| 23andMe | rs56348461 |
| SNPshot | rs56348461 |
| SNPdbe | rs56348461 |
| MSV3d | rs56348461 |
| GWAS Ctlg | rs56348461 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs56348461(C;C) |
| Alt | rs56348461(C;C) |
| Reference | Rs56348461(A;A) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.223589A>C |
| CLNSRC | |
| CLNACC | |
[PMID 6188720] Hemoglobin Tokoname [alpha 139 (HC 1) Lys leads to Thr]: a new hemoglobin variant with a slightly increased oxygen affinity.
