rs10090117
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10090117(C;C) |
| Make rs10090117(C;T) |
| Make rs10090117(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 18523725 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10090117 |
| dbSNP (classic) | rs10090117 |
| ClinGen | rs10090117 |
| ebi | rs10090117 |
| HLI | rs10090117 |
| Exac | rs10090117 |
| Gnomad | rs10090117 |
| Varsome | rs10090117 |
| LitVar | rs10090117 |
| Map | rs10090117 |
| PheGenI | rs10090117 |
| Biobank | rs10090117 |
| 1000 genomes | rs10090117 |
| hgdp | rs10090117 |
| ensembl | rs10090117 |
| geneview | rs10090117 |
| scholar | rs10090117 |
| rs10090117 | |
| pharmgkb | rs10090117 |
| gwascentral | rs10090117 |
| openSNP | rs10090117 |
| 23andMe | rs10090117 |
| SNPshot | rs10090117 |
| SNPdbe | rs10090117 |
| MSV3d | rs10090117 |
| GWAS Ctlg | rs10090117 |
| GMAF | 0.1869 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23776197] |
| Trait | Paclitaxel-induced neuropathy |
| Title | Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy. |
| Risk Allele | G |
| P-val | 4E-6 |
| Odds Ratio | 2.38 [1.64-3.44] |
