rs12020569
From SNPedia
| Merged into | rs9512491 |
| Orientation | plus |
| Stabilized | plus |
| Make rs12020569(C;C) |
| Make rs12020569(C;G) |
| Make rs12020569(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 27012736 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12020569 |
| dbSNP (classic) | rs12020569 |
| ClinGen | rs12020569 |
| ebi | rs12020569 |
| HLI | rs12020569 |
| Exac | rs12020569 |
| Gnomad | rs12020569 |
| Varsome | rs12020569 |
| LitVar | rs12020569 |
| Map | rs12020569 |
| PheGenI | rs12020569 |
| Biobank | rs12020569 |
| 1000 genomes | rs12020569 |
| hgdp | rs12020569 |
| ensembl | rs12020569 |
| geneview | rs12020569 |
| scholar | rs12020569 |
| rs12020569 | |
| pharmgkb | rs12020569 |
| gwascentral | rs12020569 |
| openSNP | rs12020569 |
| 23andMe | rs12020569 |
| SNPshot | rs12020569 |
| SNPdbe | rs12020569 |
| MSV3d | rs12020569 |
| GWAS Ctlg | rs12020569 |
| Status | Merged into rs9512491 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21314694 ]
|
| Trait | |
| Title | Genomewide Association Analysis of Symptoms of Alcohol Dependence in the Molecular Genetics of Schizophrenia (MGS2) Control Sample |
| Risk Allele | C |
| P-val | 0.000005 |
| Odds Ratio | None None |
