rs12721607
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs12721607(A;A) |
| Make rs12721607(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 119807356 |
| Gene | NR1I2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12721607 |
| dbSNP (classic) | rs12721607 |
| ClinGen | rs12721607 |
| ebi | rs12721607 |
| HLI | rs12721607 |
| Exac | rs12721607 |
| Gnomad | rs12721607 |
| Varsome | rs12721607 |
| LitVar | rs12721607 |
| Map | rs12721607 |
| PheGenI | rs12721607 |
| Biobank | rs12721607 |
| 1000 genomes | rs12721607 |
| hgdp | rs12721607 |
| ensembl | rs12721607 |
| geneview | rs12721607 |
| scholar | rs12721607 |
| rs12721607 | |
| pharmgkb | rs12721607 |
| gwascentral | rs12721607 |
| openSNP | rs12721607 |
| 23andMe | rs12721607 |
| SNPshot | rs12721607 |
| SNPdbe | rs12721607 |
| MSV3d | rs12721607 |
| GWAS Ctlg | rs12721607 |
| GMAF | 0.005969 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[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.
