rs894177
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs894177(A;A) |
| Make rs894177(A;G) |
| Make rs894177(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 143175569 |
| Gene | PBX2P1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs894177 |
| dbSNP (classic) | rs894177 |
| ClinGen | rs894177 |
| ebi | rs894177 |
| HLI | rs894177 |
| Exac | rs894177 |
| Gnomad | rs894177 |
| Varsome | rs894177 |
| LitVar | rs894177 |
| Map | rs894177 |
| PheGenI | rs894177 |
| Biobank | rs894177 |
| 1000 genomes | rs894177 |
| hgdp | rs894177 |
| ensembl | rs894177 |
| geneview | rs894177 |
| scholar | rs894177 |
| rs894177 | |
| pharmgkb | rs894177 |
| gwascentral | rs894177 |
| openSNP | rs894177 |
| 23andMe | rs894177 |
| SNPshot | rs894177 |
| SNPdbe | rs894177 |
| MSV3d | rs894177 |
| GWAS Ctlg | rs894177 |
| GMAF | 0.2452 |
| 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 | G |
| P-val | 0.000003 |
| Odds Ratio | 0.28 [NR] unit decrease |
