rs1265564
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1265564(A;A) |
| Make rs1265564(A;C) |
| Make rs1265564(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 111270654 |
| Gene | CUX2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1265564 |
| dbSNP (classic) | rs1265564 |
| ClinGen | rs1265564 |
| ebi | rs1265564 |
| HLI | rs1265564 |
| Exac | rs1265564 |
| Gnomad | rs1265564 |
| Varsome | rs1265564 |
| LitVar | rs1265564 |
| Map | rs1265564 |
| PheGenI | rs1265564 |
| Biobank | rs1265564 |
| 1000 genomes | rs1265564 |
| hgdp | rs1265564 |
| ensembl | rs1265564 |
| geneview | rs1265564 |
| scholar | rs1265564 |
| rs1265564 | |
| pharmgkb | rs1265564 |
| gwascentral | rs1265564 |
| openSNP | rs1265564 |
| 23andMe | rs1265564 |
| SNPshot | rs1265564 |
| SNPdbe | rs1265564 |
| MSV3d | rs1265564 |
| GWAS Ctlg | rs1265564 |
| GMAF | 0.1933 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 22293688 ]
|
| Trait | |
| Title | 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. |
| Risk Allele | |
| P-val | 1E-16 |
| Odds Ratio | 1.4500 None |
