rs2383378
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2383378(A;A) |
| Make rs2383378(A;C) |
| Make rs2383378(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 32813264 |
| Gene | AKAP6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2383378 |
| dbSNP (classic) | rs2383378 |
| ClinGen | rs2383378 |
| ebi | rs2383378 |
| HLI | rs2383378 |
| Exac | rs2383378 |
| Gnomad | rs2383378 |
| Varsome | rs2383378 |
| LitVar | rs2383378 |
| Map | rs2383378 |
| PheGenI | rs2383378 |
| Biobank | rs2383378 |
| 1000 genomes | rs2383378 |
| hgdp | rs2383378 |
| ensembl | rs2383378 |
| geneview | rs2383378 |
| scholar | rs2383378 |
| rs2383378 | |
| pharmgkb | rs2383378 |
| gwascentral | rs2383378 |
| openSNP | rs2383378 |
| 23andMe | rs2383378 |
| SNPshot | rs2383378 |
| SNPdbe | rs2383378 |
| MSV3d | rs2383378 |
| GWAS Ctlg | rs2383378 |
| GMAF | 0.2208 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 0.000006 |
| 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.
