rs3863377
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3863377(C;C) |
Make rs3863377(C;T) |
Make rs3863377(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 100472862 |
Gene | NR1H4 |
is a | snp |
is | mentioned by |
dbSNP | rs3863377 |
dbSNP (classic) | rs3863377 |
ClinGen | rs3863377 |
ebi | rs3863377 |
HLI | rs3863377 |
Exac | rs3863377 |
Gnomad | rs3863377 |
Varsome | rs3863377 |
LitVar | rs3863377 |
Map | rs3863377 |
PheGenI | rs3863377 |
Biobank | rs3863377 |
1000 genomes | rs3863377 |
hgdp | rs3863377 |
ensembl | rs3863377 |
geneview | rs3863377 |
scholar | rs3863377 |
rs3863377 | |
pharmgkb | rs3863377 |
gwascentral | rs3863377 |
openSNP | rs3863377 |
23andMe | rs3863377 |
SNPshot | rs3863377 |
SNPdbe | rs3863377 |
MSV3d | rs3863377 |
GWAS Ctlg | rs3863377 |
GMAF | 0.01653 |
Max Magnitude | 0 |
? | (C;C) (C;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