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rs2178146

From SNPedia

Orientationminus
Stabilizedminus
Make rs2178146(A;A)
Make rs2178146(A;G)
Make rs2178146(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position86430089
is asnp
is mentioned by
dbSNPrs2178146
ebirs2178146
HLIrs2178146
Exacrs2178146
Varsomers2178146
Maprs2178146
PheGenIrs2178146
hapmaprs2178146
1000 genomesrs2178146
hgdprs2178146
ensemblrs2178146
gopubmedrs2178146
geneviewrs2178146
scholarrs2178146
googlers2178146
pharmgkbrs2178146
gwascentralrs2178146
openSNPrs2178146
23andMers2178146
23andMe allrs2178146
SNP Nexus

SNPshotrs2178146
SNPdbers2178146
MSV3drs2178146
GWAS Ctlgrs2178146
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24121790OA-icon.png]
Trait Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined)
Title A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
Risk Allele A
P-val 1E-6
Odds Ratio 1.14 [1.09-1.2]