rs34890875
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs34890875(A;T) |
| Make rs34890875(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 176957 |
| Gene | HBA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34890875 |
| dbSNP (classic) | rs34890875 |
| ClinGen | rs34890875 |
| ebi | rs34890875 |
| HLI | rs34890875 |
| Exac | rs34890875 |
| Gnomad | rs34890875 |
| Varsome | rs34890875 |
| LitVar | rs34890875 |
| Map | rs34890875 |
| PheGenI | rs34890875 |
| Biobank | rs34890875 |
| 1000 genomes | rs34890875 |
| hgdp | rs34890875 |
| ensembl | rs34890875 |
| geneview | rs34890875 |
| scholar | rs34890875 |
| rs34890875 | |
| pharmgkb | rs34890875 |
| gwascentral | rs34890875 |
| openSNP | rs34890875 |
| 23andMe | rs34890875 |
| SNPshot | rs34890875 |
| SNPdbe | rs34890875 |
| MSV3d | rs34890875 |
| GWAS Ctlg | rs34890875 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34890875(T;T) |
| Alt | rs34890875(T;T) |
| Reference | Rs34890875(A;A) |
| Significance | Other |
| Disease | HEMOGLOBIN MIYANO |
| Variation | info |
| Gene | HBA1 |
| CLNDBN | HEMOGLOBIN MIYANO |
| Reversed | 0 |
| HGVS | NC_000016.9:g.226956A>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000017115.2, |
[PMID 2634665] Hb Miyano or alpha 41(C6)Thr----Ser: a new high oxygen affinity alpha chain variant found in an erythremic blood donor.
