rs6999631
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6999631(C;C) |
| Make rs6999631(C;G) |
| Make rs6999631(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 10228901 |
| Gene | MSRA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6999631 |
| dbSNP (classic) | rs6999631 |
| ClinGen | rs6999631 |
| ebi | rs6999631 |
| HLI | rs6999631 |
| Exac | rs6999631 |
| Gnomad | rs6999631 |
| Varsome | rs6999631 |
| LitVar | rs6999631 |
| Map | rs6999631 |
| PheGenI | rs6999631 |
| Biobank | rs6999631 |
| 1000 genomes | rs6999631 |
| hgdp | rs6999631 |
| ensembl | rs6999631 |
| geneview | rs6999631 |
| scholar | rs6999631 |
| rs6999631 | |
| pharmgkb | rs6999631 |
| gwascentral | rs6999631 |
| openSNP | rs6999631 |
| 23andMe | rs6999631 |
| SNPshot | rs6999631 |
| SNPdbe | rs6999631 |
| MSV3d | rs6999631 |
| GWAS Ctlg | rs6999631 |
| GMAF | 0.1547 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23568457 ]
|
| Trait | Bulimia nervosa |
| Title | Genetic variants associated with disordered eating. |
| Risk Allele | C |
| P-val | 8E-6 |
| Odds Ratio | .09 [0.051-0.129] unit decrease |
