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rs2149085

From SNPedia

Orientationplus
Stabilizedplus
Make rs2149085(C;C)
Make rs2149085(C;T)
Make rs2149085(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position166957622
GeneRNASET2
is asnp
is mentioned by
dbSNPrs2149085
ebirs2149085
HLIrs2149085
Exacrs2149085
Varsomers2149085
Maprs2149085
PheGenIrs2149085
hapmaprs2149085
1000 genomesrs2149085
hgdprs2149085
ensemblrs2149085
gopubmedrs2149085
geneviewrs2149085
scholarrs2149085
googlers2149085
pharmgkbrs2149085
gwascentralrs2149085
openSNPrs2149085
23andMers2149085
23andMe allrs2149085
SNP Nexus

SNPshotrs2149085
SNPdbers2149085
MSV3drs2149085
GWAS Ctlgrs2149085
GMAF0.393
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23850713]
Trait Crohn's disease
Title Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
Risk Allele T
P-val 8E-12
Odds Ratio 1.34 [1.23-1.45]