rs6929404
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6929404(A;A) |
| Make rs6929404(A;C) |
| Make rs6929404(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 135132889 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6929404 |
| dbSNP (classic) | rs6929404 |
| ClinGen | rs6929404 |
| ebi | rs6929404 |
| HLI | rs6929404 |
| Exac | rs6929404 |
| Gnomad | rs6929404 |
| Varsome | rs6929404 |
| LitVar | rs6929404 |
| Map | rs6929404 |
| PheGenI | rs6929404 |
| Biobank | rs6929404 |
| 1000 genomes | rs6929404 |
| hgdp | rs6929404 |
| ensembl | rs6929404 |
| geneview | rs6929404 |
| scholar | rs6929404 |
| rs6929404 | |
| pharmgkb | rs6929404 |
| gwascentral | rs6929404 |
| openSNP | rs6929404 |
| 23andMe | rs6929404 |
| SNPshot | rs6929404 |
| SNPdbe | rs6929404 |
| MSV3d | rs6929404 |
| GWAS Ctlg | rs6929404 |
| GMAF | 0.3012 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 17592125
] Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.
[PMID 18667698] DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
[PMID 20401335] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
