rs6591182
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6591182(G;G) |
| Make rs6591182(G;T) |
| Make rs6591182(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 65582285 |
| Gene | EHBP1L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6591182 |
| dbSNP (classic) | rs6591182 |
| ClinGen | rs6591182 |
| ebi | rs6591182 |
| HLI | rs6591182 |
| Exac | rs6591182 |
| Gnomad | rs6591182 |
| Varsome | rs6591182 |
| LitVar | rs6591182 |
| Map | rs6591182 |
| PheGenI | rs6591182 |
| Biobank | rs6591182 |
| 1000 genomes | rs6591182 |
| hgdp | rs6591182 |
| ensembl | rs6591182 |
| geneview | rs6591182 |
| scholar | rs6591182 |
| rs6591182 | |
| pharmgkb | rs6591182 |
| gwascentral | rs6591182 |
| openSNP | rs6591182 |
| 23andMe | rs6591182 |
| SNPshot | rs6591182 |
| SNPdbe | rs6591182 |
| MSV3d | rs6591182 |
| GWAS Ctlg | rs6591182 |
| GMAF | 0.4316 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | 9E-7 |
| Odds Ratio | 0.54 [NR] unit increase |
