rs957788
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs957788(A;A) |
| Make rs957788(A;G) |
| Make rs957788(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 107604872 |
| Gene | FAM155A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs957788 |
| dbSNP (classic) | rs957788 |
| ClinGen | rs957788 |
| ebi | rs957788 |
| HLI | rs957788 |
| Exac | rs957788 |
| Gnomad | rs957788 |
| Varsome | rs957788 |
| LitVar | rs957788 |
| Map | rs957788 |
| PheGenI | rs957788 |
| Biobank | rs957788 |
| 1000 genomes | rs957788 |
| hgdp | rs957788 |
| ensembl | rs957788 |
| geneview | rs957788 |
| scholar | rs957788 |
| rs957788 | |
| pharmgkb | rs957788 |
| gwascentral | rs957788 |
| openSNP | rs957788 |
| 23andMe | rs957788 |
| SNPshot | rs957788 |
| SNPdbe | rs957788 |
| MSV3d | rs957788 |
| GWAS Ctlg | rs957788 |
| GMAF | 0.287 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21079607 ]
|
| Trait | |
| Title | A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa |
| Risk Allele | |
| P-val | 0.000008 |
| Odds Ratio | None None |
