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Rs206468

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Orientationminus
Make rs206468(A;A)
Make rs206468(A;G)
Make rs206468(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position10296941
is asnp
is mentioned by
dbSNPrs206468
PheGenIrs206468
nextbiors206468
hapmaprs206468
1000 genomesrs206468
hgdprs206468
ensemblrs206468
gopubmedrs206468
geneviewrs206468
scholarrs206468
googlers206468
pharmgkbrs206468
gwascentralrs206468
openSNPrs206468
23andMers206468
23andMe allrs206468
SNP Nexus

SNPshotrs206468
SNPdbers206468
MSV3drs206468
GMAF0.3338
Max Magnitude
GWAS
SNP rs11209003,rs11209002,rs206468
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