rs2461823
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2461823(A;A) |
| Make rs2461823(A;G) |
| Make rs2461823(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 119801278 |
| Gene | NR1I2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2461823 |
| dbSNP (classic) | rs2461823 |
| ClinGen | rs2461823 |
| ebi | rs2461823 |
| HLI | rs2461823 |
| Exac | rs2461823 |
| Gnomad | rs2461823 |
| Varsome | rs2461823 |
| LitVar | rs2461823 |
| Map | rs2461823 |
| PheGenI | rs2461823 |
| Biobank | rs2461823 |
| 1000 genomes | rs2461823 |
| hgdp | rs2461823 |
| ensembl | rs2461823 |
| geneview | rs2461823 |
| scholar | rs2461823 |
| rs2461823 | |
| pharmgkb | rs2461823 |
| gwascentral | rs2461823 |
| openSNP | rs2461823 |
| 23andMe | rs2461823 |
| SNPshot | rs2461823 |
| SNPdbe | rs2461823 |
| MSV3d | rs2461823 |
| GWAS Ctlg | rs2461823 |
| GMAF | 0.3871 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[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 18381611] Investigation of associations between the pregnane-X receptor gene (NR1I2) and Crohn's disease in Canadian children using a gene-wide haplotype-based approach.
