rs12991836
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12991836(A;A) |
| Make rs12991836(A;C) |
| Make rs12991836(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 2 |
| Position | 144383974 |
| Gene | ZEB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12991836 |
| dbSNP (classic) | rs12991836 |
| ClinGen | rs12991836 |
| ebi | rs12991836 |
| HLI | rs12991836 |
| Exac | rs12991836 |
| Gnomad | rs12991836 |
| Varsome | rs12991836 |
| LitVar | rs12991836 |
| Map | rs12991836 |
| PheGenI | rs12991836 |
| Biobank | rs12991836 |
| 1000 genomes | rs12991836 |
| hgdp | rs12991836 |
| ensembl | rs12991836 |
| geneview | rs12991836 |
| scholar | rs12991836 |
| rs12991836 | |
| pharmgkb | rs12991836 |
| gwascentral | rs12991836 |
| openSNP | rs12991836 |
| 23andMe | rs12991836 |
| SNPshot | rs12991836 |
| SNPdbe | rs12991836 |
| MSV3d | rs12991836 |
| GWAS Ctlg | rs12991836 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 1E-8 |
| Odds Ratio | 1.08 [1.05-1.11] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
