rs391760
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs391760(A;A) |
| Make rs391760(A;C) |
| Make rs391760(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 144031781 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs391760 |
| dbSNP (classic) | rs391760 |
| ClinGen | rs391760 |
| ebi | rs391760 |
| HLI | rs391760 |
| Exac | rs391760 |
| Gnomad | rs391760 |
| Varsome | rs391760 |
| LitVar | rs391760 |
| Map | rs391760 |
| PheGenI | rs391760 |
| Biobank | rs391760 |
| 1000 genomes | rs391760 |
| hgdp | rs391760 |
| ensembl | rs391760 |
| geneview | rs391760 |
| scholar | rs391760 |
| rs391760 | |
| pharmgkb | rs391760 |
| gwascentral | rs391760 |
| openSNP | rs391760 |
| 23andMe | rs391760 |
| SNPshot | rs391760 |
| SNPdbe | rs391760 |
| MSV3d | rs391760 |
| GWAS Ctlg | rs391760 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24322204] |
| Trait | Bipolar disorder (body mass index interaction) |
| Title | Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2. |
| Risk Allele | |
| P-val | 2E-6 |
| Odds Ratio | NR NR |
