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rs11894081

From SNPedia

Orientationplus
Stabilizedplus
Make rs11894081(G;G)
Make rs11894081(G;T)
Make rs11894081(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position5523876
is asnp
is mentioned by
dbSNPrs11894081
ebirs11894081
HLIrs11894081
Exacrs11894081
Varsomers11894081
Maprs11894081
PheGenIrs11894081
hapmaprs11894081
1000 genomesrs11894081
hgdprs11894081
ensemblrs11894081
gopubmedrs11894081
geneviewrs11894081
scholarrs11894081
googlers11894081
pharmgkbrs11894081
gwascentralrs11894081
openSNPrs11894081
23andMers11894081
23andMe allrs11894081
SNP Nexus

SNPshotrs11894081
SNPdbers11894081
MSV3drs11894081
GWAS Ctlgrs11894081
GMAF0.4353
Max Magnitude
GWAS snp
PMID [PMID 23266558]
Trait Crohn's disease
Title A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
Risk Allele T
P-val 4E-9
Odds Ratio 1.22 [1.2-1.22]