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rs9258260

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9258260(C;T)
Make rs9258260(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29755384
is asnp
is mentioned by
dbSNPrs9258260
ebirs9258260
HLIrs9258260
Exacrs9258260
Varsomers9258260
Maprs9258260
PheGenIrs9258260
hapmaprs9258260
1000 genomesrs9258260
hgdprs9258260
ensemblrs9258260
gopubmedrs9258260
geneviewrs9258260
scholarrs9258260
googlers9258260
pharmgkbrs9258260
gwascentralrs9258260
openSNPrs9258260
23andMers9258260
23andMe allrs9258260
SNP Nexus

SNPshotrs9258260
SNPdbers9258260
MSV3drs9258260
GWAS Ctlgrs9258260
GMAF0.1373
Max Magnitude0
? (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 2E-10
Odds Ratio 1.4500 None