rs2699783
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2699783(C;C) |
| Make rs2699783(C;T) |
| Make rs2699783(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 66031567 |
| Gene | LOC105369168 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2699783 |
| dbSNP (classic) | rs2699783 |
| ClinGen | rs2699783 |
| ebi | rs2699783 |
| HLI | rs2699783 |
| Exac | rs2699783 |
| Gnomad | rs2699783 |
| Varsome | rs2699783 |
| LitVar | rs2699783 |
| Map | rs2699783 |
| PheGenI | rs2699783 |
| Biobank | rs2699783 |
| 1000 genomes | rs2699783 |
| hgdp | rs2699783 |
| ensembl | rs2699783 |
| geneview | rs2699783 |
| scholar | rs2699783 |
| rs2699783 | |
| pharmgkb | rs2699783 |
| gwascentral | rs2699783 |
| openSNP | rs2699783 |
| 23andMe | rs2699783 |
| SNPshot | rs2699783 |
| SNPdbe | rs2699783 |
| MSV3d | rs2699783 |
| GWAS Ctlg | rs2699783 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| 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 | 7E-6 |
| Odds Ratio | NR NR |
