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rs10947261

From SNPedia

Orientationplus
Stabilizedplus
Make rs10947261(G;G)
Make rs10947261(G;T)
Make rs10947261(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32405455
GeneBTNL2
is asnp
is mentioned by
dbSNPrs10947261
ebirs10947261
HLIrs10947261
Exacrs10947261
Varsomers10947261
Maprs10947261
PheGenIrs10947261
hapmaprs10947261
1000 genomesrs10947261
hgdprs10947261
ensemblrs10947261
gopubmedrs10947261
geneviewrs10947261
scholarrs10947261
googlers10947261
pharmgkbrs10947261
gwascentralrs10947261
openSNPrs10947261
23andMers10947261
23andMe allrs10947261
SNP Nexus

SNPshotrs10947261
SNPdbers10947261
MSV3drs10947261
GWAS Ctlgrs10947261
GMAF0.1644
Max Magnitude
? (G;G) (G;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 3E-12
Odds Ratio 1.36 [1.25-1.49]