rs12037606
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 2 | 1.52x risk of developing Crohn's disease |
(A;G) | 1.5 | 1.22x risk of developing Crohn's disease |
(C;C) | 0 | |
(G;G) | 1 | Normal risk of developing Crohn's disease |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 172929262 |
is a | snp |
is | mentioned by |
dbSNP | rs12037606 |
dbSNP (classic) | rs12037606 |
ClinGen | rs12037606 |
ebi | rs12037606 |
HLI | rs12037606 |
Exac | rs12037606 |
Gnomad | rs12037606 |
Varsome | rs12037606 |
LitVar | rs12037606 |
Map | rs12037606 |
PheGenI | rs12037606 |
Biobank | rs12037606 |
1000 genomes | rs12037606 |
hgdp | rs12037606 |
ensembl | rs12037606 |
geneview | rs12037606 |
scholar | rs12037606 |
rs12037606 | |
pharmgkb | rs12037606 |
gwascentral | rs12037606 |
openSNP | rs12037606 |
23andMe | rs12037606 |
SNPshot | rs12037606 |
SNPdbe | rs12037606 |
MSV3d | rs12037606 |
GWAS Ctlg | rs12037606 |
GMAF | 0.3388 |
Max Magnitude | 2 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs12037606 has been reported in a large study to be associated with Crohn's disease.
The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.22 (CI 1.07-1.40), and for homozygotes, 1.52 (CI 1.28-1.82). [PMID 17554300]