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rs12567232

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 2 Increased risk for Crohn's Disease
(A;G) 2 Increased risk for Crohn's Disease
(G;G) 0 normal
ReferenceGRCh38 38.1/141
Chromosome1
Position67262335
is asnp
is mentioned by
dbSNPrs12567232
ebirs12567232
HLIrs12567232
Exacrs12567232
Varsomers12567232
Maprs12567232
PheGenIrs12567232
hapmaprs12567232
1000 genomesrs12567232
hgdprs12567232
ensemblrs12567232
gopubmedrs12567232
geneviewrs12567232
scholarrs12567232
googlers12567232
pharmgkbrs12567232
gwascentralrs12567232
openSNPrs12567232
23andMers12567232
23andMe allrs12567232
SNP Nexus

SNPshotrs12567232
SNPdbers12567232
MSV3drs12567232
GWAS Ctlgrs12567232
GMAF0.3632
Max Magnitude2
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs12567232
PubMedID [PMID 17804789OA-icon.png]
Condition Crohn's disease
Gene IL23R
Risk Allele A
pValue 1.00E-008
OR 1.38
95% CI 1.23-1.53



GET Evidence
rs12567232
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.328125
summary