rs17496827
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17496827(A;A) |
| Make rs17496827(A;C) |
| Make rs17496827(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 222488727 |
| Gene | SGPP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17496827 |
| dbSNP (classic) | rs17496827 |
| ClinGen | rs17496827 |
| ebi | rs17496827 |
| HLI | rs17496827 |
| Exac | rs17496827 |
| Gnomad | rs17496827 |
| Varsome | rs17496827 |
| LitVar | rs17496827 |
| Map | rs17496827 |
| PheGenI | rs17496827 |
| Biobank | rs17496827 |
| 1000 genomes | rs17496827 |
| hgdp | rs17496827 |
| ensembl | rs17496827 |
| geneview | rs17496827 |
| scholar | rs17496827 |
| rs17496827 | |
| pharmgkb | rs17496827 |
| gwascentral | rs17496827 |
| openSNP | rs17496827 |
| 23andMe | rs17496827 |
| SNPshot | rs17496827 |
| SNPdbe | rs17496827 |
| MSV3d | rs17496827 |
| GWAS Ctlg | rs17496827 |
| GMAF | 0.4803 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23568457 ]
|
| Trait | Anorexia nervosa |
| Title | Genetic variants associated with disordered eating. |
| Risk Allele | C |
| P-val | 7E-6 |
| Odds Ratio | .04 [0.024-0.06] unit decrease |
