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rs3091338

From SNPedia

Orientationplus
Stabilizedplus
Make rs3091338(C;C)
Make rs3091338(C;T)
Make rs3091338(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132067045
is asnp
is mentioned by
dbSNPrs3091338
ebirs3091338
HLIrs3091338
Exacrs3091338
Varsomers3091338
Maprs3091338
PheGenIrs3091338
hapmaprs3091338
1000 genomesrs3091338
hgdprs3091338
ensemblrs3091338
gopubmedrs3091338
geneviewrs3091338
scholarrs3091338
googlers3091338
pharmgkbrs3091338
gwascentralrs3091338
openSNPrs3091338
23andMers3091338
23andMe allrs3091338
SNP Nexus

SNPshotrs3091338
SNPdbers3091338
MSV3drs3091338
GWAS Ctlgrs3091338
GMAF0.2094
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22412388OA-icon.png]
Trait
Title A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
Risk Allele T
P-val 4E-8
Odds Ratio 1.2300 None