Rs11209002

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Orientationplus
Make rs11209002(C;C)
Make rs11209002(C;T)
Make rs11209002(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position67124778
GeneC1orf141
is asnp
is mentioned by
dbSNPrs11209002
Exacrs11209002
PheGenIrs11209002
nextbiors11209002
hapmaprs11209002
1000 genomesrs11209002
hgdprs11209002
ensemblrs11209002
gopubmedrs11209002
geneviewrs11209002
scholarrs11209002
googlers11209002
pharmgkbrs11209002
gwascentralrs11209002
openSNPrs11209002
23andMers11209002
23andMe allrs11209002
SNP Nexus

SNPshotrs11209002
SNPdbers11209002
MSV3drs11209002
GMAF0.2195
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs11209002
PubMedID [PMID 17804789OA-icon.png]
Condition Crohn's disease
Gene IL23R
Risk Allele
pValue 2.00E-007
OR 2.56
95% CI 1.75-3.70



GET Evidence
rs11209002
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.726562
summary