rs766432
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs766432(A;A) |
| Make rs766432(A;C) |
| Make rs766432(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 60492835 |
| Gene | BCL11A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs766432 |
| dbSNP (classic) | rs766432 |
| ClinGen | rs766432 |
| ebi | rs766432 |
| HLI | rs766432 |
| Exac | rs766432 |
| Gnomad | rs766432 |
| Varsome | rs766432 |
| LitVar | rs766432 |
| Map | rs766432 |
| PheGenI | rs766432 |
| Biobank | rs766432 |
| 1000 genomes | rs766432 |
| hgdp | rs766432 |
| ensembl | rs766432 |
| geneview | rs766432 |
| scholar | rs766432 |
| rs766432 | |
| pharmgkb | rs766432 |
| gwascentral | rs766432 |
| openSNP | rs766432 |
| 23andMe | rs766432 |
| SNPshot | rs766432 |
| SNPdbe | rs766432 |
| MSV3d | rs766432 |
| GWAS Ctlg | rs766432 |
| GMAF | 0.2153 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19924444] |
| Trait | Beta thalassemia/hemoglobin E disease |
| Title | A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E |
| Risk Allele | |
| P-val | 1E-10 |
| Odds Ratio | 2.80 [2.04-3.84] |
[PMID 20018918
] Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster
| GWAS snp | |
|---|---|
| PMID | [PMID 20183929] |
| Trait | Beta thalassemia/hemoglobin E disease |
| Title | A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. |
| Risk Allele | |
| P-val | 1E-10 |
| Odds Ratio | 2.8000 [2.04-3.84] |
[PMID 19966804] Geographical genomics of human leukocyte gene expression variation in southern Morocco.
[PMID 21326311] Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
[PMID 22686296] The XmnI and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian beta-Thalassemia Patients.
| GWAS snp | |
|---|---|
| PMID | [PMID 23406172]
|
| Trait | Sickle cell anemia (haemolysis) |
| Title | Genetic determinants of haemolysis in sickle cell anaemia. |
| Risk Allele | |
| P-val | 9E-7 |
| Odds Ratio | .22 NR unit increase |
[PMID 32387854] The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese β-thalassemia patients.
