rs7138843
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7138843(A;A) |
Make rs7138843(A;T) |
Make rs7138843(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 100536917 |
Gene | NR1H4 |
is a | snp |
is | mentioned by |
dbSNP | rs7138843 |
dbSNP (classic) | rs7138843 |
ClinGen | rs7138843 |
ebi | rs7138843 |
HLI | rs7138843 |
Exac | rs7138843 |
Gnomad | rs7138843 |
Varsome | rs7138843 |
LitVar | rs7138843 |
Map | rs7138843 |
PheGenI | rs7138843 |
Biobank | rs7138843 |
1000 genomes | rs7138843 |
hgdp | rs7138843 |
ensembl | rs7138843 |
geneview | rs7138843 |
scholar | rs7138843 |
rs7138843 | |
pharmgkb | rs7138843 |
gwascentral | rs7138843 |
openSNP | rs7138843 |
23andMe | rs7138843 |
SNPshot | rs7138843 |
SNPdbe | rs7138843 |
MSV3d | rs7138843 |
GWAS Ctlg | rs7138843 |
GMAF | 0.281 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 22929053] Association of genetic variation in the NR1H4 gene, encoding the nuclear bile acid receptor FXR, with inflammatory bowel disease