rs12509991
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12509991(C;C) |
| Make rs12509991(C;T) |
| Make rs12509991(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 4 |
| Position | 126075715 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12509991 |
| dbSNP (classic) | rs12509991 |
| ClinGen | rs12509991 |
| ebi | rs12509991 |
| HLI | rs12509991 |
| Exac | rs12509991 |
| Gnomad | rs12509991 |
| Varsome | rs12509991 |
| LitVar | rs12509991 |
| Map | rs12509991 |
| PheGenI | rs12509991 |
| Biobank | rs12509991 |
| 1000 genomes | rs12509991 |
| hgdp | rs12509991 |
| ensembl | rs12509991 |
| geneview | rs12509991 |
| scholar | rs12509991 |
| rs12509991 | |
| pharmgkb | rs12509991 |
| gwascentral | rs12509991 |
| openSNP | rs12509991 |
| 23andMe | rs12509991 |
| SNPshot | rs12509991 |
| SNPdbe | rs12509991 |
| MSV3d | rs12509991 |
| GWAS Ctlg | rs12509991 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 25628645 ]
|
| Trait | Response to Homoharringtonine (cytotoxicity) |
| Title | Identification of genetic variants or genes that are associated with Homoharringtonine (HHT) response through a genome-wide association study in human lymphoblastoid cell lines (LCLs). |
| Risk Allele | |
| P-val | 3E-7 |
| Odds Ratio | |
