rs13077017
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13077017(C;C) |
| Make rs13077017(C;T) |
| Make rs13077017(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 58120049 |
| Gene | FLNB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13077017 |
| dbSNP (classic) | rs13077017 |
| ClinGen | rs13077017 |
| ebi | rs13077017 |
| HLI | rs13077017 |
| Exac | rs13077017 |
| Gnomad | rs13077017 |
| Varsome | rs13077017 |
| LitVar | rs13077017 |
| Map | rs13077017 |
| PheGenI | rs13077017 |
| Biobank | rs13077017 |
| 1000 genomes | rs13077017 |
| hgdp | rs13077017 |
| ensembl | rs13077017 |
| geneview | rs13077017 |
| scholar | rs13077017 |
| rs13077017 | |
| pharmgkb | rs13077017 |
| gwascentral | rs13077017 |
| openSNP | rs13077017 |
| 23andMe | rs13077017 |
| SNPshot | rs13077017 |
| SNPdbe | rs13077017 |
| MSV3d | rs13077017 |
| GWAS Ctlg | rs13077017 |
| GMAF | 0.1474 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23568457 |
| Trait | Eating disorders (purging via substances) |
| Title | Genetic variants associated with disordered eating. |
| Risk Allele | C |
| P-val | 1E-6 |
| Odds Ratio | .07 [0.044-0.102] unit decrease |
