rs9822268
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9822268(A;A) |
Make rs9822268(A;G) |
Make rs9822268(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 49682296 |
Gene | APEH |
is a | snp |
is | mentioned by |
dbSNP | rs9822268 |
dbSNP (classic) | rs9822268 |
ClinGen | rs9822268 |
ebi | rs9822268 |
HLI | rs9822268 |
Exac | rs9822268 |
Gnomad | rs9822268 |
Varsome | rs9822268 |
LitVar | rs9822268 |
Map | rs9822268 |
PheGenI | rs9822268 |
Biobank | rs9822268 |
1000 genomes | rs9822268 |
hgdp | rs9822268 |
ensembl | rs9822268 |
geneview | rs9822268 |
scholar | rs9822268 |
rs9822268 | |
pharmgkb | rs9822268 |
gwascentral | rs9822268 |
openSNP | rs9822268 |
23andMe | rs9822268 |
SNPshot | rs9822268 |
SNPdbe | rs9822268 |
MSV3d | rs9822268 |
GWAS Ctlg | rs9822268 |
GMAF | 0.2351 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21297633] |
Trait | |
Title | Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 |
Risk Allele | A |
P-val | 2E-17 |
Odds Ratio | 1.2100 [1.16-1.26] |
[PMID 17804789] Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.