Rs13361189

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is asnp
is mentioned by
dbSNPrs13361189
nextbiors13361189
hapmaprs13361189
1000 genomesrs13361189
hgdprs13361189
ensemblrs13361189
gopubmedrs13361189
scholarrs13361189
googlers13361189
pharmgkbrs13361189
gwascentralrs13361189
openSNPrs13361189
23andMers13361189
23andMe allrs13361189
SNP Nexus

SNPshotrs13361189
SNPdbers13361189
MSV3drs13361189
Chromosome5
Orientationplus
Position150223387
ReferenceGRCh37 37.1/131
Max Magnitude2.6
Geno Mag Summary
(C;C) 2.6 2.6x increased risk for Crohn's disease
(C;T) 1.3 1.3x increased risk for Crohn's disease
(T;T) 0 normal
? (C;C) (C;T) (T;T) 28
rs13361189 is a SNP in the IRGM gene.

A study including 557 Crohn's disease (CD) patients, 425 ulcerative colitis (UC) patients, and 672 ethnically matched Spanish controls as well as a meta-analysis concluded that rs13361189(C) was associated with CD (p=1.07 x 10(-19), pooled odds ratio 1.34) and UC (p=0.0069, pooled odds ratio 1.16).[PMID 19491842]

spittoon Each copy of a C at rs13361189 increases a person's risk of developing Crohn's disease 1.33 times compared to someone with two copies of a T

GWAS
SNP rs13361189
PubMedID [PMID 17554261]
Condition Crohn's disease
Gene IRGM
Risk Allele
pValue 2.00E-010
OR 1.38
95% CI 1.15-1.66


OMIM612278
DescINFLAMMATORY BOWEL DISEASE 19; IBD19
Variant
Relatedalso
OMIM608212
DescIMMUNITY-RELATED GTPase FAMILY, M; IRGM
Variant
Relatedalso
PharmGKBPA162356573
Name
AnnotationGWAS results: Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility (Initial Sample Size: 1,748 cases, 2,938 controls; Replication Sample Size: 1,182 cases, 2,024 controls). This variant is associated with Crohn's disease.
Gene-
Featue
EvidencePubMed ID:17554261; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesCrohn Disease
Curation LevelNon-Curated


[PMID 19953089] Differences in genetic background between active smokers, passive smokers, and non-smokers with Crohn's disease

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