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rs11465788

From SNPedia

Orientationplus
Stabilizedplus
Make rs11465788(C;C)
Make rs11465788(C;T)
Make rs11465788(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position67182611
GeneIL23R
is asnp
is mentioned by
dbSNPrs11465788
ebirs11465788
HLIrs11465788
Exacrs11465788
Varsomers11465788
Maprs11465788
PheGenIrs11465788
hapmaprs11465788
1000 genomesrs11465788
hgdprs11465788
ensemblrs11465788
gopubmedrs11465788
geneviewrs11465788
scholarrs11465788
googlers11465788
pharmgkbrs11465788
gwascentralrs11465788
openSNPrs11465788
23andMers11465788
23andMe allrs11465788
SNP Nexus

SNPshotrs11465788
SNPdbers11465788
MSV3drs11465788
GWAS Ctlgrs11465788
GMAF0.4784
Max Magnitude

[PMID 19700857] Contribution of rs11465788 in IL23R gene to Crohn's disease susceptibility and phenotype in Chinese population [PMID 21304977OA-icon.png] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.