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rs11465770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 normal Crohn's Disease risk
(C;T) 1.5 possibly lower risk of Crohn's Disease (OR=0.30)
(T;T) 1.5 possibly lower risk of Crohn's Disease (OR=0.30)
ReferenceGRCh38 38.1/141
Chromosome1
Position67168280
GeneIL23R
is asnp
is mentioned by
dbSNPrs11465770
ebirs11465770
HLIrs11465770
Exacrs11465770
Varsomers11465770
Maprs11465770
PheGenIrs11465770
hapmaprs11465770
1000 genomesrs11465770
hgdprs11465770
ensemblrs11465770
gopubmedrs11465770
geneviewrs11465770
scholarrs11465770
googlers11465770
pharmgkbrs11465770
gwascentralrs11465770
openSNPrs11465770
23andMers11465770
23andMe allrs11465770
SNP Nexus

SNPshotrs11465770
SNPdbers11465770
MSV3drs11465770
GWAS Ctlgrs11465770
GMAF0.0404
Max Magnitude1.5
? (C;C) (C;T) (T;T) 28
Contribution of rs11465788 in IL23R gene to Crohn's disease susceptibility and phenotype in Chinese population. [PMID 19700857] Found that T allele may be protective against Crohn's disease in Chinese.