Rs13361189

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs13361189
hapmaprs13361189
hgdprs13361189
ensemblrs13361189
gopubmedrs13361189
scholarrs13361189
googlers13361189
pharmgkbrs13361189
hgvbaseg2prs13361189
medrefsnprs13361189
23andMers13361189
SNP Nexus

Chromosome5
Orientationplus
Position150203580
GenotypeEffect
rs13361189(C;C)2.6x increased risk for Crohn's disease
rs13361189(C;T)1.3x increased risk for Crohn's disease
rs13361189(T;T)normal


Genotypes Magnitude Summary
Rs13361189(C;C) 2.62.6 2.6x increased risk for Crohn's disease
Rs13361189(C;T) 1.31.3 1.3x increased risk for Crohn's disease
Rs13361189(T;T) 00 normal

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

? (C;C) (C;T) (T;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


Related to INFLAMMATORY BOWEL DISEASE 19; IBD19 according to omim 612278. See also


Related to IMMUNITY-RELATED GTPase FAMILY, M; IRGM according to omim 608212. See also


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