rs271738
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs271738(A;A) |
| Make rs271738(A;G) |
| Make rs271738(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 234527144 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs271738 |
| dbSNP (classic) | rs271738 |
| ClinGen | rs271738 |
| ebi | rs271738 |
| HLI | rs271738 |
| Exac | rs271738 |
| Gnomad | rs271738 |
| Varsome | rs271738 |
| LitVar | rs271738 |
| Map | rs271738 |
| PheGenI | rs271738 |
| Biobank | rs271738 |
| 1000 genomes | rs271738 |
| hgdp | rs271738 |
| ensembl | rs271738 |
| geneview | rs271738 |
| scholar | rs271738 |
| rs271738 | |
| pharmgkb | rs271738 |
| gwascentral | rs271738 |
| openSNP | rs271738 |
| 23andMe | rs271738 |
| SNPshot | rs271738 |
| SNPdbe | rs271738 |
| MSV3d | rs271738 |
| GWAS Ctlg | rs271738 |
| GMAF | 0.3586 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | A |
| P-val | 0.000005 |
| Odds Ratio | 1.3200 None |
