rs12488820
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12488820(C;C) |
Make rs12488820(C;T) |
Make rs12488820(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 119783222 |
Gene | NR1I2 |
is a | snp |
is | mentioned by |
dbSNP | rs12488820 |
dbSNP (classic) | rs12488820 |
ClinGen | rs12488820 |
ebi | rs12488820 |
HLI | rs12488820 |
Exac | rs12488820 |
Gnomad | rs12488820 |
Varsome | rs12488820 |
LitVar | rs12488820 |
Map | rs12488820 |
PheGenI | rs12488820 |
Biobank | rs12488820 |
1000 genomes | rs12488820 |
hgdp | rs12488820 |
ensembl | rs12488820 |
geneview | rs12488820 |
scholar | rs12488820 |
rs12488820 | |
pharmgkb | rs12488820 |
gwascentral | rs12488820 |
openSNP | rs12488820 |
23andMe | rs12488820 |
SNPshot | rs12488820 |
SNPdbe | rs12488820 |
MSV3d | rs12488820 |
GWAS Ctlg | rs12488820 |
GMAF | 0.4807 |
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