rs34807671
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs34807671(C;T) |
| Make rs34807671(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5253282 |
| Gene | HBG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34807671 |
| dbSNP (classic) | rs34807671 |
| ClinGen | rs34807671 |
| ebi | rs34807671 |
| HLI | rs34807671 |
| Exac | rs34807671 |
| Gnomad | rs34807671 |
| Varsome | rs34807671 |
| LitVar | rs34807671 |
| Map | rs34807671 |
| PheGenI | rs34807671 |
| Biobank | rs34807671 |
| 1000 genomes | rs34807671 |
| hgdp | rs34807671 |
| ensembl | rs34807671 |
| geneview | rs34807671 |
| scholar | rs34807671 |
| rs34807671 | |
| pharmgkb | rs34807671 |
| gwascentral | rs34807671 |
| openSNP | rs34807671 |
| 23andMe | rs34807671 |
| SNPshot | rs34807671 |
| SNPdbe | rs34807671 |
| MSV3d | rs34807671 |
| GWAS Ctlg | rs34807671 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs34807671(T;T) |
| Alt | rs34807671(T;T) |
| Reference | Rs34807671(C;C) |
| Significance | Other |
| Disease | HEMOGLOBIN F (ONODA) |
| Variation | info |
| Gene | HBG2 |
| CLNDBN | HEMOGLOBIN F (ONODA) |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5274512G>A |
| CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016128.1, |
[PMID 1703139] Hb F-Onoda or alpha 2G gamma 2(146)(HC3)His----Tyr, a newly discovered fetal hemoglobin variant in a Japanese newborn.
