rs34579351
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs34579351(A;G) |
| Make rs34579351(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5226608 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34579351 |
| dbSNP (classic) | rs34579351 |
| ClinGen | rs34579351 |
| ebi | rs34579351 |
| HLI | rs34579351 |
| Exac | rs34579351 |
| Gnomad | rs34579351 |
| Varsome | rs34579351 |
| LitVar | rs34579351 |
| Map | rs34579351 |
| PheGenI | rs34579351 |
| Biobank | rs34579351 |
| 1000 genomes | rs34579351 |
| hgdp | rs34579351 |
| ensembl | rs34579351 |
| geneview | rs34579351 |
| scholar | rs34579351 |
| rs34579351 | |
| pharmgkb | rs34579351 |
| gwascentral | rs34579351 |
| openSNP | rs34579351 |
| 23andMe | rs34579351 |
| SNPshot | rs34579351 |
| SNPdbe | rs34579351 |
| MSV3d | rs34579351 |
| GWAS Ctlg | rs34579351 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34579351(G;G) |
| Alt | rs34579351(G;G) |
| Reference | Rs34579351(A;A) |
| Significance | Other |
| Disease | HEMOGLOBIN CHANDIGARH |
| Variation | info |
| Gene | HBB |
| CLNDBN | HEMOGLOBIN CHANDIGARH |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5247838T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016296.2, |
[PMID 2634672] Hb Chandigarh or alpha 2 beta 2(94)(FG1)Asp----Gly observed in an Indian family.
[PMID 15481898] Late emergence of polycythemia in a case of Hb Chandigarh [beta94(FG1)Asp-->Gly].
