rs17725255
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs17725255(C;C) |
| Make rs17725255(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 18098487 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17725255 |
| dbSNP (classic) | rs17725255 |
| ClinGen | rs17725255 |
| ebi | rs17725255 |
| HLI | rs17725255 |
| Exac | rs17725255 |
| Gnomad | rs17725255 |
| Varsome | rs17725255 |
| LitVar | rs17725255 |
| Map | rs17725255 |
| PheGenI | rs17725255 |
| Biobank | rs17725255 |
| 1000 genomes | rs17725255 |
| hgdp | rs17725255 |
| ensembl | rs17725255 |
| geneview | rs17725255 |
| scholar | rs17725255 |
| rs17725255 | |
| pharmgkb | rs17725255 |
| gwascentral | rs17725255 |
| openSNP | rs17725255 |
| 23andMe | rs17725255 |
| SNPshot | rs17725255 |
| SNPdbe | rs17725255 |
| MSV3d | rs17725255 |
| GWAS Ctlg | rs17725255 |
| GMAF | 0.124 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21079607 ]
|
| Trait | Anorexia nervosa |
| Title | A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | None None |
[PMID 23568457] Genetic variants associated with disordered eating.
[PMID 21079607] A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.
