rs116896199
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs116896199(A;A) |
| Make rs116896199(A;G) |
| Make rs116896199(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 61531817 |
| Gene | CDH4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs116896199 |
| dbSNP (classic) | rs116896199 |
| ClinGen | rs116896199 |
| ebi | rs116896199 |
| HLI | rs116896199 |
| Exac | rs116896199 |
| Gnomad | rs116896199 |
| Varsome | rs116896199 |
| LitVar | rs116896199 |
| Map | rs116896199 |
| PheGenI | rs116896199 |
| Biobank | rs116896199 |
| 1000 genomes | rs116896199 |
| hgdp | rs116896199 |
| ensembl | rs116896199 |
| geneview | rs116896199 |
| scholar | rs116896199 |
| rs116896199 | |
| pharmgkb | rs116896199 |
| gwascentral | rs116896199 |
| openSNP | rs116896199 |
| 23andMe | rs116896199 |
| SNPshot | rs116896199 |
| SNPdbe | rs116896199 |
| MSV3d | rs116896199 |
| GWAS Ctlg | rs116896199 |
| 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 | 5E-6 |
| Odds Ratio | NR NR |
