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rs6785049

From SNPedia

Orientationplus
Stabilizedplus
Make rs6785049(A;A)
Make rs6785049(A;G)
Make rs6785049(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position119814886
GeneNR1I2
is asnp
is mentioned by
dbSNPrs6785049
ebirs6785049
HLIrs6785049
Exacrs6785049
Varsomers6785049
Maprs6785049
PheGenIrs6785049
hapmaprs6785049
1000 genomesrs6785049
hgdprs6785049
ensemblrs6785049
gopubmedrs6785049
geneviewrs6785049
scholarrs6785049
googlers6785049
pharmgkbrs6785049
gwascentralrs6785049
openSNPrs6785049
23andMers6785049
23andMe allrs6785049
SNP Nexus

SNPshotrs6785049
SNPdbers6785049
MSV3drs6785049
GWAS Ctlgrs6785049
GMAF0.4444
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19940802] The nuclear receptor PXR gene variants are associated with liver injury in nonalcoholic fatty liver disease


[PMID 19739075] Polymorphisms in genes of the steroid receptor superfamily modify postmenopausal breast cancer risk associated with menopausal hormone therapy

[PMID 19958310] The influence of common gene variants of the xenobiotic receptor (PXR) in genetic susceptibility to intrahepatic cholestasis of pregnancy

[PMID 20836841OA-icon.png] Polymorphisms in NFkB, PXR, LXR and risk of colorectal cancer in a prospective study of Danes


[PMID 16952547] Polymorphisms in the steroid and xenobiotic receptor gene influence survival in primary sclerosing cholangitis.


[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.