rs4479806
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs4479806(A;A) |
| Make rs4479806(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 26723674 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4479806 |
| dbSNP (classic) | rs4479806 |
| ClinGen | rs4479806 |
| ebi | rs4479806 |
| HLI | rs4479806 |
| Exac | rs4479806 |
| Gnomad | rs4479806 |
| Varsome | rs4479806 |
| LitVar | rs4479806 |
| Map | rs4479806 |
| PheGenI | rs4479806 |
| Biobank | rs4479806 |
| 1000 genomes | rs4479806 |
| hgdp | rs4479806 |
| ensembl | rs4479806 |
| geneview | rs4479806 |
| scholar | rs4479806 |
| rs4479806 | |
| pharmgkb | rs4479806 |
| gwascentral | rs4479806 |
| openSNP | rs4479806 |
| 23andMe | rs4479806 |
| SNPshot | rs4479806 |
| SNPdbe | rs4479806 |
| MSV3d | rs4479806 |
| GWAS Ctlg | rs4479806 |
| GMAF | 0.1157 |
| 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 | 0.000008 |
| Odds Ratio | None None |
