rs1186868
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs1186868(A;A) |
| Make rs1186868(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 61764103 |
| Gene | LOC107985767 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1186868 |
| dbSNP (classic) | rs1186868 |
| ClinGen | rs1186868 |
| ebi | rs1186868 |
| HLI | rs1186868 |
| Exac | rs1186868 |
| Gnomad | rs1186868 |
| Varsome | rs1186868 |
| LitVar | rs1186868 |
| Map | rs1186868 |
| PheGenI | rs1186868 |
| Biobank | rs1186868 |
| 1000 genomes | rs1186868 |
| hgdp | rs1186868 |
| ensembl | rs1186868 |
| geneview | rs1186868 |
| scholar | rs1186868 |
| rs1186868 | |
| pharmgkb | rs1186868 |
| gwascentral | rs1186868 |
| openSNP | rs1186868 |
| 23andMe | rs1186868 |
| SNPshot | rs1186868 |
| SNPdbe | rs1186868 |
| MSV3d | rs1186868 |
| GWAS Ctlg | rs1186868 |
| GMAF | 0.05556 |
| Max Magnitude | 0 |
| GWAS | |
|---|---|
| SNP | rs1186868 |
| PubMedID | [PMID 18245381 ]
|
| Condition | Fetal hemoglobin levels |
| Gene | BCL11A |
| Risk Allele | T |
| pValue | 7.00E-035 |
| OR | 0.48 |
| 95% CI | NR) SD decrease in Hb |
[PMID 19474294] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
