Have questions? Visit https://www.reddit.com/r/SNPedia

rs9267911

From SNPedia

Orientationplus
Stabilizedplus
Make rs9267911(C;C)
Make rs9267911(C;T)
Make rs9267911(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32237333
is asnp
is mentioned by
dbSNPrs9267911
ebirs9267911
HLIrs9267911
Exacrs9267911
Varsomers9267911
Maprs9267911
PheGenIrs9267911
hapmaprs9267911
1000 genomesrs9267911
hgdprs9267911
ensemblrs9267911
gopubmedrs9267911
geneviewrs9267911
scholarrs9267911
googlers9267911
pharmgkbrs9267911
gwascentralrs9267911
openSNPrs9267911
23andMers9267911
23andMe allrs9267911
SNP Nexus

SNPshotrs9267911
SNPdbers9267911
MSV3drs9267911
GWAS Ctlgrs9267911
GMAF0.416
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 3E-7
Odds Ratio 1.50 [1.29-1.76]