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rs12037606

From SNPedia

Orientationplus
Stabilizedplus
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
ReferenceGRCh38 38.1/141
Chromosome1
Position172929262
is asnp
is mentioned by
dbSNPrs12037606
ebirs12037606
HLIrs12037606
Exacrs12037606
Varsomers12037606
Maprs12037606
PheGenIrs12037606
hapmaprs12037606
1000 genomesrs12037606
hgdprs12037606
ensemblrs12037606
gopubmedrs12037606
geneviewrs12037606
scholarrs12037606
googlers12037606
pharmgkbrs12037606
gwascentralrs12037606
openSNPrs12037606
23andMers12037606
23andMe allrs12037606
SNP Nexus

SNPshotrs12037606
SNPdbers12037606
MSV3drs12037606
GWAS Ctlgrs12037606
GMAF0.3388
Max Magnitude2
? (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 17554300OA-icon.png]