rs2910032
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2910032(C;C) |
| Make rs2910032(C;T) |
| Make rs2910032(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 153160794 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2910032 |
| dbSNP (classic) | rs2910032 |
| ClinGen | rs2910032 |
| ebi | rs2910032 |
| HLI | rs2910032 |
| Exac | rs2910032 |
| Gnomad | rs2910032 |
| Varsome | rs2910032 |
| LitVar | rs2910032 |
| Map | rs2910032 |
| PheGenI | rs2910032 |
| Biobank | rs2910032 |
| 1000 genomes | rs2910032 |
| hgdp | rs2910032 |
| ensembl | rs2910032 |
| geneview | rs2910032 |
| scholar | rs2910032 |
| rs2910032 | |
| pharmgkb | rs2910032 |
| gwascentral | rs2910032 |
| openSNP | rs2910032 |
| 23andMe | rs2910032 |
| SNPshot | rs2910032 |
| SNPdbe | rs2910032 |
| MSV3d | rs2910032 |
| GWAS Ctlg | rs2910032 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23974872 |
| Trait | Schizophrenia |
| Title | Genome-wide association analysis identifies 13 new risk loci for schizophrenia. |
| Risk Allele | C |
| P-val | 4E-8 |
| Odds Ratio | 1.08 [1.05-1.11] |
