rs12073837
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12073837(C;C) |
| Make rs12073837(C;T) |
| Make rs12073837(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 220836863 |
| Gene | HLX-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12073837 |
| dbSNP (classic) | rs12073837 |
| ClinGen | rs12073837 |
| ebi | rs12073837 |
| HLI | rs12073837 |
| Exac | rs12073837 |
| Gnomad | rs12073837 |
| Varsome | rs12073837 |
| LitVar | rs12073837 |
| Map | rs12073837 |
| PheGenI | rs12073837 |
| Biobank | rs12073837 |
| 1000 genomes | rs12073837 |
| hgdp | rs12073837 |
| ensembl | rs12073837 |
| geneview | rs12073837 |
| scholar | rs12073837 |
| rs12073837 | |
| pharmgkb | rs12073837 |
| gwascentral | rs12073837 |
| openSNP | rs12073837 |
| 23andMe | rs12073837 |
| SNPshot | rs12073837 |
| SNPdbe | rs12073837 |
| MSV3d | rs12073837 |
| GWAS Ctlg | rs12073837 |
| GMAF | 0.258 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21326311 ]
|
| Trait | |
| Title | Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients |
| Risk Allele | T |
| P-val | 0.000002 |
| Odds Ratio | 1.3900 [0.82-1.96] unit increase |
