rs2472671
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2472671(C;C) |
Make rs2472671(C;T) |
Make rs2472671(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 119784198 |
Gene | NR1I2 |
is a | snp |
is | mentioned by |
dbSNP | rs2472671 |
dbSNP (classic) | rs2472671 |
ClinGen | rs2472671 |
ebi | rs2472671 |
HLI | rs2472671 |
Exac | rs2472671 |
Gnomad | rs2472671 |
Varsome | rs2472671 |
LitVar | rs2472671 |
Map | rs2472671 |
PheGenI | rs2472671 |
Biobank | rs2472671 |
1000 genomes | rs2472671 |
hgdp | rs2472671 |
ensembl | rs2472671 |
geneview | rs2472671 |
scholar | rs2472671 |
rs2472671 | |
pharmgkb | rs2472671 |
gwascentral | rs2472671 |
openSNP | rs2472671 |
23andMe | rs2472671 |
SNPshot | rs2472671 |
SNPdbe | rs2472671 |
MSV3d | rs2472671 |
GWAS Ctlg | rs2472671 |
GMAF | 0.2153 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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