rs1523127
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1523127(G;G) |
Make rs1523127(G;T) |
Make rs1523127(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 119782192 |
Gene | NR1I2 |
is a | snp |
is | mentioned by |
dbSNP | rs1523127 |
dbSNP (classic) | rs1523127 |
ClinGen | rs1523127 |
ebi | rs1523127 |
HLI | rs1523127 |
Exac | rs1523127 |
Gnomad | rs1523127 |
Varsome | rs1523127 |
LitVar | rs1523127 |
Map | rs1523127 |
PheGenI | rs1523127 |
Biobank | rs1523127 |
1000 genomes | rs1523127 |
hgdp | rs1523127 |
ensembl | rs1523127 |
geneview | rs1523127 |
scholar | rs1523127 |
rs1523127 | |
pharmgkb | rs1523127 |
gwascentral | rs1523127 |
openSNP | rs1523127 |
23andMe | rs1523127 |
SNPshot | rs1523127 |
SNPdbe | rs1523127 |
MSV3d | rs1523127 |
GWAS Ctlg | rs1523127 |
GMAF | 0.4578 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
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Gene variants associated with deep vein thrombosis.[PMID 18349091]
Updated analysis of gene variants associated with deep vein thrombosis.[PMID 20124536]
[PMID 20354687] Explaining variability in ciclosporin exposure in adult kidney transplant recipients.
[PMID 21245992] Polymorphisms in NF-kappaB, PXR, LXR, PPARgamma and risk of inflammatory bowel disease.
[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.