Rs1186868
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1186868 |
| PheGenI | rs1186868 |
| nextbio | rs1186868 |
| hapmap | rs1186868 |
| 1000 genomes | rs1186868 |
| hgdp | rs1186868 |
| ensembl | rs1186868 |
| gopubmed | rs1186868 |
| geneview | rs1186868 |
| scholar | rs1186868 |
| rs1186868 | |
| pharmgkb | rs1186868 |
| gwascentral | rs1186868 |
| openSNP | rs1186868 |
| 23andMe | rs1186868 |
| 23andMe all | rs1186868 |
| SNP Nexus | |
| SNPshot | rs1186868 |
| SNPdbe | rs1186868 |
| MSV3d | rs1186868 |
| Chromosome | 2 |
| Orientation | plus |
| GMAF | 0.0554 |
| Position | 61991238 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs1186868(A;A) |
| Make rs1186868(A;G) |
| 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.
| GET Evidence | |
|---|---|
| rs1186868 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.03125 |
| summary | |
