rs3814057
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3814057(A;A) |
| Make rs3814057(A;C) |
| Make rs3814057(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 119818407 |
| Gene | NR1I2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3814057 |
| dbSNP (classic) | rs3814057 |
| ClinGen | rs3814057 |
| ebi | rs3814057 |
| HLI | rs3814057 |
| Exac | rs3814057 |
| Gnomad | rs3814057 |
| Varsome | rs3814057 |
| LitVar | rs3814057 |
| Map | rs3814057 |
| PheGenI | rs3814057 |
| Biobank | rs3814057 |
| 1000 genomes | rs3814057 |
| hgdp | rs3814057 |
| ensembl | rs3814057 |
| geneview | rs3814057 |
| scholar | rs3814057 |
| rs3814057 | |
| pharmgkb | rs3814057 |
| gwascentral | rs3814057 |
| openSNP | rs3814057 |
| 23andMe | rs3814057 |
| SNPshot | rs3814057 |
| SNPdbe | rs3814057 |
| MSV3d | rs3814057 |
| GWAS Ctlg | rs3814057 |
| GMAF | 0.3255 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 19940802] The nuclear receptor PXR gene variants are associated with liver injury in nonalcoholic fatty liver disease
[PMID 19958310] The influence of common gene variants of the xenobiotic receptor (PXR) in genetic susceptibility to intrahepatic cholestasis of pregnancy
[PMID 21830270] Pregnane X receptor (PXR/NR1I2) gene haplotypes modulate susceptibility to inflammatory bowel disease.
[PMID 21954916] Variants of the human NR1I2 (PXR) locus in chronic periodontitis.
