rs11669592
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11669592(A;A) |
| Make rs11669592(A;G) |
| Make rs11669592(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 3318512 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11669592 |
| dbSNP (classic) | rs11669592 |
| ClinGen | rs11669592 |
| ebi | rs11669592 |
| HLI | rs11669592 |
| Exac | rs11669592 |
| Gnomad | rs11669592 |
| Varsome | rs11669592 |
| LitVar | rs11669592 |
| Map | rs11669592 |
| PheGenI | rs11669592 |
| Biobank | rs11669592 |
| 1000 genomes | rs11669592 |
| hgdp | rs11669592 |
| ensembl | rs11669592 |
| geneview | rs11669592 |
| scholar | rs11669592 |
| rs11669592 | |
| pharmgkb | rs11669592 |
| gwascentral | rs11669592 |
| openSNP | rs11669592 |
| 23andMe | rs11669592 |
| SNPshot | rs11669592 |
| SNPdbe | rs11669592 |
| MSV3d | rs11669592 |
| GWAS Ctlg | rs11669592 |
| GMAF | 0.4444 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20708005 ]
|
| Trait | |
| Title | Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease |
| Risk Allele | A |
| P-val | 0.000004 |
| Odds Ratio | 1.31 [NR] unit decrease |
