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rs9988642

From SNPedia

Orientationplus
Stabilizedplus
Make rs9988642(C;C)
Make rs9988642(C;T)
Make rs9988642(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position67260421
GeneIL23R
is asnp
is mentioned by
dbSNPrs9988642
ebirs9988642
HLIrs9988642
Exacrs9988642
Varsomers9988642
Maprs9988642
PheGenIrs9988642
hapmaprs9988642
1000 genomesrs9988642
hgdprs9988642
ensemblrs9988642
gopubmedrs9988642
geneviewrs9988642
scholarrs9988642
googlers9988642
pharmgkbrs9988642
gwascentralrs9988642
openSNPrs9988642
23andMers9988642
23andMe allrs9988642
SNP Nexus

SNPshotrs9988642
SNPdbers9988642
MSV3drs9988642
GWAS Ctlgrs9988642
GMAF0.1084
Max Magnitude
GWAS
SNP rs9988642
PubMedID [PMID 17804789OA-icon.png]
Condition Crohn's disease
Gene IL23R
Risk Allele
pValue 1.00E-008
OR 1.38
95% CI 1.23-1.53



GET Evidence
rs9988642
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.101562
summary