rs9267911
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9267911(C;C) |
Make rs9267911(C;T) |
Make rs9267911(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32237333 |
is a | snp |
is | mentioned by |
dbSNP | rs9267911 |
dbSNP (classic) | rs9267911 |
ClinGen | rs9267911 |
ebi | rs9267911 |
HLI | rs9267911 |
Exac | rs9267911 |
Gnomad | rs9267911 |
Varsome | rs9267911 |
LitVar | rs9267911 |
Map | rs9267911 |
PheGenI | rs9267911 |
Biobank | rs9267911 |
1000 genomes | rs9267911 |
hgdp | rs9267911 |
ensembl | rs9267911 |
geneview | rs9267911 |
scholar | rs9267911 |
rs9267911 | |
pharmgkb | rs9267911 |
gwascentral | rs9267911 |
openSNP | rs9267911 |
23andMe | rs9267911 |
SNPshot | rs9267911 |
SNPdbe | rs9267911 |
MSV3d | rs9267911 |
GWAS Ctlg | rs9267911 |
GMAF | 0.416 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23266558] |
Trait | Crohn's disease |
Title | A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population. |
Risk Allele | T |
P-val | 3E-7 |
Odds Ratio | 1.50 [1.29-1.76] |