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rs2927438

From SNPedia

Orientationplus
Stabilizedplus
Make rs2927438(A;A)
Make rs2927438(A;G)
Make rs2927438(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44738850
is asnp
is mentioned by
dbSNPrs2927438
ebirs2927438
HLIrs2927438
Exacrs2927438
Varsomers2927438
Maprs2927438
PheGenIrs2927438
hapmaprs2927438
1000 genomesrs2927438
hgdprs2927438
ensemblrs2927438
gopubmedrs2927438
geneviewrs2927438
scholarrs2927438
googlers2927438
pharmgkbrs2927438
gwascentralrs2927438
openSNPrs2927438
23andMers2927438
23andMe allrs2927438
SNP Nexus

SNPshotrs2927438
SNPdbers2927438
MSV3drs2927438
GWAS Ctlgrs2927438
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 C
P-val 2E-6
Odds Ratio 1.16 [1.1-1.25]