rs34776279
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs34776279(A;A) |
| Make rs34776279(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 176798 |
| Gene | HBA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34776279 |
| dbSNP (classic) | rs34776279 |
| ClinGen | rs34776279 |
| ebi | rs34776279 |
| HLI | rs34776279 |
| Exac | rs34776279 |
| Gnomad | rs34776279 |
| Varsome | rs34776279 |
| LitVar | rs34776279 |
| Map | rs34776279 |
| PheGenI | rs34776279 |
| Biobank | rs34776279 |
| 1000 genomes | rs34776279 |
| hgdp | rs34776279 |
| ensembl | rs34776279 |
| geneview | rs34776279 |
| scholar | rs34776279 |
| rs34776279 | |
| pharmgkb | rs34776279 |
| gwascentral | rs34776279 |
| openSNP | rs34776279 |
| 23andMe | rs34776279 |
| SNPshot | rs34776279 |
| SNPdbe | rs34776279 |
| MSV3d | rs34776279 |
| GWAS Ctlg | rs34776279 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34776279(A;A) |
| Alt | rs34776279(A;A) |
| Reference | Rs34776279(G;G) |
| Significance | Other |
| Disease | HEMOGLOBIN SHUANGFENG |
| Variation | info |
| Gene | HBA1 |
| CLNDBN | HEMOGLOBIN SHUANGFENG |
| Reversed | 0 |
| HGVS | NC_000016.9:g.226797G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000017156.2, |
[PMID 3932017] Oxygen equilibrium characteristics of four abnormal hemoglobins found in Hunan.
[PMID 7338471] Hemoglobin Shuangfeng (alpha 27 (B8) Glu substituting for Lys): a new unstable hemoglobin variant.
