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rs2695121

From SNPedia

Orientationplus
Stabilizedplus
Make rs2695121(C;C)
Make rs2695121(C;T)
Make rs2695121(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position50377484
GeneNR1H2
is asnp
is mentioned by
dbSNPrs2695121
dbSNP (classic)rs2695121
ClinGenrs2695121
ebirs2695121
HLIrs2695121
Exacrs2695121
Gnomadrs2695121
Varsomers2695121
LitVarrs2695121
Maprs2695121
PheGenIrs2695121
Biobankrs2695121
1000 genomesrs2695121
hgdprs2695121
ensemblrs2695121
geneviewrs2695121
scholarrs2695121
googlers2695121
pharmgkbrs2695121
gwascentralrs2695121
openSNPrs2695121
23andMers2695121
SNPshotrs2695121
SNPdbers2695121
MSV3drs2695121
GWAS Ctlgrs2695121
GMAF0.2539
Max Magnitude0

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


[PMID 20939869OA-icon.png] Suggestive evidence of associations between liver X receptor beta polymorphisms with type 2 diabetes mellitus and obesity in three cohort studies: HUNT 2 (Norway), MONICA (France) and HELENA (Europe)


[PMID 22029530OA-icon.png] A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia


[PMID 17108812] Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity.


[PMID 18597895] Gene-gene interaction between heme oxygenase-1 and liver X receptor-beta and Alzheimer's disease risk.


[PMID 19292929OA-icon.png] Functional and genetic analysis in type 2 diabetes of liver X receptor alleles--a cohort study.


[PMID 21245992OA-icon.png] Polymorphisms in NF-kappaB, PXR, LXR, PPARgamma and risk of inflammatory bowel disease.


[PMID 23838803] Association of liver X receptors (LXRs) genetic variants to gallbladder cancer susceptibility


[PMID 24100084] Lack of association between LXRα and LXRβ gene polymorphisms and prevalence of metabolic syndrome: a case-control study of an Iranian population


[PMID 24863943] A multigenic approach to evaluate genetic variants of PLCE1, LXRs, MMPs, TIMP, and CYP genes in gallbladder cancer predisposition


[PMID 28244008] Liver X Receptor Genes Variants Modulate ALS Phenotype.