rs17135859
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17135859(C;C) |
| Make rs17135859(C;T) |
| Make rs17135859(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 113660957 |
| Gene | LOC107986441 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17135859 |
| dbSNP (classic) | rs17135859 |
| ClinGen | rs17135859 |
| ebi | rs17135859 |
| HLI | rs17135859 |
| Exac | rs17135859 |
| Gnomad | rs17135859 |
| Varsome | rs17135859 |
| LitVar | rs17135859 |
| Map | rs17135859 |
| PheGenI | rs17135859 |
| Biobank | rs17135859 |
| 1000 genomes | rs17135859 |
| hgdp | rs17135859 |
| ensembl | rs17135859 |
| geneview | rs17135859 |
| scholar | rs17135859 |
| rs17135859 | |
| pharmgkb | rs17135859 |
| gwascentral | rs17135859 |
| openSNP | rs17135859 |
| 23andMe | rs17135859 |
| SNPshot | rs17135859 |
| SNPdbe | rs17135859 |
| MSV3d | rs17135859 |
| GWAS Ctlg | rs17135859 |
| GMAF | 0.1322 |
| 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 | C |
| P-val | 0.000008 |
| Odds Ratio | 0.9700 [0.54-1.40] unit increase |
