rs35724
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs35724(C;C) |
Make rs35724(C;G) |
Make rs35724(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 100561600 |
Gene | NR1H4 |
is a | snp |
is | mentioned by |
dbSNP | rs35724 |
dbSNP (classic) | rs35724 |
ClinGen | rs35724 |
ebi | rs35724 |
HLI | rs35724 |
Exac | rs35724 |
Gnomad | rs35724 |
Varsome | rs35724 |
LitVar | rs35724 |
Map | rs35724 |
PheGenI | rs35724 |
Biobank | rs35724 |
1000 genomes | rs35724 |
hgdp | rs35724 |
ensembl | rs35724 |
geneview | rs35724 |
scholar | rs35724 |
rs35724 | |
pharmgkb | rs35724 |
gwascentral | rs35724 |
openSNP | rs35724 |
23andMe | rs35724 |
SNPshot | rs35724 |
SNPdbe | rs35724 |
MSV3d | rs35724 |
GWAS Ctlg | rs35724 |
GMAF | 0.4467 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 22929053] Association of genetic variation in the NR1H4 gene, encoding the nuclear bile acid receptor FXR, with inflammatory bowel disease
[PMID 25242139] Association of FXR gene variants with cholelithiasis
[PMID 31062417] Impact of farnesoid X receptor SNPs on hepatic decompensation and mortality in cirrhotic patients with portal hypertension.