rs410644
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs410644(G;G) |
| Make rs410644(G;T) |
| Make rs410644(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 81791715 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs410644 |
| dbSNP (classic) | rs410644 |
| ClinGen | rs410644 |
| ebi | rs410644 |
| HLI | rs410644 |
| Exac | rs410644 |
| Gnomad | rs410644 |
| Varsome | rs410644 |
| LitVar | rs410644 |
| Map | rs410644 |
| PheGenI | rs410644 |
| Biobank | rs410644 |
| 1000 genomes | rs410644 |
| hgdp | rs410644 |
| ensembl | rs410644 |
| geneview | rs410644 |
| scholar | rs410644 |
| rs410644 | |
| pharmgkb | rs410644 |
| gwascentral | rs410644 |
| openSNP | rs410644 |
| 23andMe | rs410644 |
| SNPshot | rs410644 |
| SNPdbe | rs410644 |
| MSV3d | rs410644 |
| GWAS Ctlg | rs410644 |
| GMAF | 0.3393 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | 0.000007 |
| Odds Ratio | None None |
