rs469339
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs469339(A;A) |
| Make rs469339(A;G) |
| Make rs469339(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 94812833 |
| Gene | MCTP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs469339 |
| dbSNP (classic) | rs469339 |
| ClinGen | rs469339 |
| ebi | rs469339 |
| HLI | rs469339 |
| Exac | rs469339 |
| Gnomad | rs469339 |
| Varsome | rs469339 |
| LitVar | rs469339 |
| Map | rs469339 |
| PheGenI | rs469339 |
| Biobank | rs469339 |
| 1000 genomes | rs469339 |
| hgdp | rs469339 |
| ensembl | rs469339 |
| geneview | rs469339 |
| scholar | rs469339 |
| rs469339 | |
| pharmgkb | rs469339 |
| gwascentral | rs469339 |
| openSNP | rs469339 |
| 23andMe | rs469339 |
| SNPshot | rs469339 |
| SNPdbe | rs469339 |
| MSV3d | rs469339 |
| GWAS Ctlg | rs469339 |
| GMAF | 0.08448 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23568457 ]
|
| Trait | Anorexia nervosa |
| Title | Genetic variants associated with disordered eating. |
| Risk Allele | A |
| P-val | 3E-6 |
| Odds Ratio | .14 [0.083-0.205] unit decrease |
