rs12071951
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12071951(G;G) |
| Make rs12071951(G;T) |
| Make rs12071951(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 96648359 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12071951 |
| dbSNP (classic) | rs12071951 |
| ClinGen | rs12071951 |
| ebi | rs12071951 |
| HLI | rs12071951 |
| Exac | rs12071951 |
| Gnomad | rs12071951 |
| Varsome | rs12071951 |
| LitVar | rs12071951 |
| Map | rs12071951 |
| PheGenI | rs12071951 |
| Biobank | rs12071951 |
| 1000 genomes | rs12071951 |
| hgdp | rs12071951 |
| ensembl | rs12071951 |
| geneview | rs12071951 |
| scholar | rs12071951 |
| rs12071951 | |
| pharmgkb | rs12071951 |
| gwascentral | rs12071951 |
| openSNP | rs12071951 |
| 23andMe | rs12071951 |
| SNPshot | rs12071951 |
| SNPdbe | rs12071951 |
| MSV3d | rs12071951 |
| GWAS Ctlg | rs12071951 |
| GMAF | 0.2805 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22688191 ]
|
| Trait | |
| Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
| Risk Allele | |
| P-val | 5E-7 |
| Odds Ratio | 1.1400 None |
