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rs11103429

From SNPedia

Orientationplus
Stabilizedplus
Make rs11103429(A;A)
Make rs11103429(A;G)
Make rs11103429(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position134614732
is asnp
is mentioned by
dbSNPrs11103429
ebirs11103429
HLIrs11103429
Exacrs11103429
Varsomers11103429
Maprs11103429
PheGenIrs11103429
hapmaprs11103429
1000 genomesrs11103429
hgdprs11103429
ensemblrs11103429
gopubmedrs11103429
geneviewrs11103429
scholarrs11103429
googlers11103429
pharmgkbrs11103429
gwascentralrs11103429
openSNPrs11103429
23andMers11103429
23andMe allrs11103429
SNP Nexus

SNPshotrs11103429
SNPdbers11103429
MSV3drs11103429
GWAS Ctlgrs11103429
GMAF0.08402
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23665963OA-icon.png]
Trait Crohn's disease (need for surgery)
Title Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.
Risk Allele G
P-val 6E-6
Odds Ratio 3.60 [2.10-6.30]