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rs1523127

From SNPedia

Orientationminus
Stabilizedminus
Make rs1523127(G;G)
Make rs1523127(G;T)
Make rs1523127(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position119782192
GeneNR1I2
is asnp
is mentioned by
dbSNPrs1523127
ebirs1523127
HLIrs1523127
Exacrs1523127
Varsomers1523127
Maprs1523127
PheGenIrs1523127
hapmaprs1523127
1000 genomesrs1523127
hgdprs1523127
ensemblrs1523127
gopubmedrs1523127
geneviewrs1523127
scholarrs1523127
googlers1523127
pharmgkbrs1523127
gwascentralrs1523127
openSNPrs1523127
23andMers1523127
23andMe allrs1523127
SNP Nexus

SNPshotrs1523127
SNPdbers1523127
MSV3drs1523127
GWAS Ctlgrs1523127
GMAF0.4578
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 20836841OA-icon.png] Polymorphisms in NFkB, PXR, LXR and risk of colorectal cancer in a prospective study of Danes

Gene variants associated with deep vein thrombosis.[PMID 18349091]

Updated analysis of gene variants associated with deep vein thrombosis.[PMID 20124536]

[PMID 20354687OA-icon.png] Explaining variability in ciclosporin exposure in adult kidney transplant recipients.

[PMID 21245992OA-icon.png] 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.