rs2276707
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2276707(C;C) |
Make rs2276707(C;T) |
Make rs2276707(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 119815306 |
Gene | NR1I2 |
is a | snp |
is | mentioned by |
dbSNP | rs2276707 |
dbSNP (classic) | rs2276707 |
ClinGen | rs2276707 |
ebi | rs2276707 |
HLI | rs2276707 |
Exac | rs2276707 |
Gnomad | rs2276707 |
Varsome | rs2276707 |
LitVar | rs2276707 |
Map | rs2276707 |
PheGenI | rs2276707 |
Biobank | rs2276707 |
1000 genomes | rs2276707 |
hgdp | rs2276707 |
ensembl | rs2276707 |
geneview | rs2276707 |
scholar | rs2276707 |
rs2276707 | |
pharmgkb | rs2276707 |
gwascentral | rs2276707 |
openSNP | rs2276707 |
23andMe | rs2276707 |
SNPshot | rs2276707 |
SNPdbe | rs2276707 |
MSV3d | rs2276707 |
GWAS Ctlg | rs2276707 |
GMAF | 0.3026 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20836841] Polymorphisms in NFkB, PXR, LXR and risk of colorectal cancer in a prospective study of Danes
[PMID 17828778] Role of the PXR gene locus in inflammatory bowel diseases.
[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.
[PMID 23462807] Single-nucleotide polymorphisms associated with outcome in metastatic renal cell carcinoma treated with sunitinib.