rs2896019
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2896019(G;G) |
| Make rs2896019(G;T) |
| Make rs2896019(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 43937814 |
| Gene | PNPLA3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2896019 |
| dbSNP (classic) | rs2896019 |
| ClinGen | rs2896019 |
| ebi | rs2896019 |
| HLI | rs2896019 |
| Exac | rs2896019 |
| Gnomad | rs2896019 |
| Varsome | rs2896019 |
| LitVar | rs2896019 |
| Map | rs2896019 |
| PheGenI | rs2896019 |
| Biobank | rs2896019 |
| 1000 genomes | rs2896019 |
| hgdp | rs2896019 |
| ensembl | rs2896019 |
| geneview | rs2896019 |
| scholar | rs2896019 |
| rs2896019 | |
| pharmgkb | rs2896019 |
| gwascentral | rs2896019 |
| openSNP | rs2896019 |
| 23andMe | rs2896019 |
| SNPshot | rs2896019 |
| SNPdbe | rs2896019 |
| MSV3d | rs2896019 |
| GWAS Ctlg | rs2896019 |
| GMAF | 0.2755 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23535911] |
| Trait | Non-alcoholic fatty liver disease |
| Title | Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan. |
| Risk Allele | G |
| P-val | 2E-20 |
| Odds Ratio | 2.02 [1.60-2.56] |
[PMID 22543885
] The association of genetic variants with hepatic steatosis in patients with genotype 1 chronic hepatitis C infection.
[PMID 24831885] Genetic Variants in the PNPLA3 Gene Are Associated with Nonalcoholic Steatohepatitis
| GWAS snp | |
|---|---|
| PMID | [PMID 20139978] |
| Trait | Hematological and biochemical traits |
| Title | Genome-wide association study of hematological and biochemical traits in a Japanese population. |
| Risk Allele | G |
| P-val | 2E-12 |
| Odds Ratio | .09 [0.061-0.109] unit increase |
[PMID 29385134] Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers.
