rs34988734
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs34988734(C;T) |
| Make rs34988734(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 177101 |
| Gene | HBA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34988734 |
| dbSNP (classic) | rs34988734 |
| ClinGen | rs34988734 |
| ebi | rs34988734 |
| HLI | rs34988734 |
| Exac | rs34988734 |
| Gnomad | rs34988734 |
| Varsome | rs34988734 |
| LitVar | rs34988734 |
| Map | rs34988734 |
| PheGenI | rs34988734 |
| Biobank | rs34988734 |
| 1000 genomes | rs34988734 |
| hgdp | rs34988734 |
| ensembl | rs34988734 |
| geneview | rs34988734 |
| scholar | rs34988734 |
| rs34988734 | |
| pharmgkb | rs34988734 |
| gwascentral | rs34988734 |
| openSNP | rs34988734 |
| 23andMe | rs34988734 |
| SNPshot | rs34988734 |
| SNPdbe | rs34988734 |
| MSV3d | rs34988734 |
| GWAS Ctlg | rs34988734 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34988734(T;T) |
| Alt | rs34988734(T;T) |
| Reference | Rs34988734(C;C) |
| Significance | Other |
| Disease | HEMOGLOBIN VILLEURBANNE |
| Variation | info |
| Gene | HBA1 |
| CLNDBN | HEMOGLOBIN VILLEURBANNE |
| Reversed | 0 |
| HGVS | NC_000016.9:g.227100C>T |
| CLNSRC | HBVAR OMIM Allelic Variant |
| CLNACC | RCV000017232.2, |
[PMID 9269086] Combined mass spectrometric methods for the characterization of human hemoglobin variants localized within alpha T9 peptide: identification of Hb Villeurbanne alpha 89 (FG1) His-->Tyr.
