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rs9348876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs9348876(C;T)
Make rs9348876(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31607499
is asnp
is mentioned by
dbSNPrs9348876
ebirs9348876
HLIrs9348876
Exacrs9348876
Varsomers9348876
Maprs9348876
PheGenIrs9348876
hapmaprs9348876
1000 genomesrs9348876
hgdprs9348876
ensemblrs9348876
gopubmedrs9348876
geneviewrs9348876
scholarrs9348876
googlers9348876
pharmgkbrs9348876
gwascentralrs9348876
openSNPrs9348876
23andMers9348876
23andMe allrs9348876
SNP Nexus

SNPshotrs9348876
SNPdbers9348876
MSV3drs9348876
GWAS Ctlgrs9348876
GMAF0.1107
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22936669]
Trait Crohn's disease
Title A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
Risk Allele T
P-val 3E-6
Odds Ratio 1.41 [1.22-1.63]


[PMID 20064070OA-icon.png] Multistage genomewide association study identifies a locus at 1q41 associated with rate of HIV-1 disease progression to clinical AIDS.