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rs2461823

From SNPedia

Orientationminus
Stabilizedminus
Make rs2461823(A;A)
Make rs2461823(A;G)
Make rs2461823(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position119801278
GeneNR1I2
is asnp
is mentioned by
dbSNPrs2461823
ebirs2461823
HLIrs2461823
Exacrs2461823
Varsomers2461823
Maprs2461823
PheGenIrs2461823
hapmaprs2461823
1000 genomesrs2461823
hgdprs2461823
ensemblrs2461823
gopubmedrs2461823
geneviewrs2461823
scholarrs2461823
googlers2461823
pharmgkbrs2461823
gwascentralrs2461823
openSNPrs2461823
23andMers2461823
23andMe allrs2461823
SNP Nexus

SNPshotrs2461823
SNPdbers2461823
MSV3drs2461823
GWAS Ctlgrs2461823
GMAF0.3871
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 19958310] The influence of common gene variants of the xenobiotic receptor (PXR) in genetic susceptibility to intrahepatic cholestasis of pregnancy


[PMID 18381611] Investigation of associations between the pregnane-X receptor gene (NR1I2) and Crohn's disease in Canadian children using a gene-wide haplotype-based approach.


GET Evidence
rs2461823
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.5625
summary