Have questions? Visit https://www.reddit.com/r/SNPedia

rs2342002

From SNPedia

Orientationplus
Stabilizedplus
Make rs2342002(C;C)
Make rs2342002(C;T)
Make rs2342002(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position61285855
is asnp
is mentioned by
dbSNPrs2342002
ebirs2342002
HLIrs2342002
Exacrs2342002
Varsomers2342002
Maprs2342002
PheGenIrs2342002
hapmaprs2342002
1000 genomesrs2342002
hgdprs2342002
ensemblrs2342002
gopubmedrs2342002
geneviewrs2342002
scholarrs2342002
googlers2342002
pharmgkbrs2342002
gwascentralrs2342002
openSNPrs2342002
23andMers2342002
23andMe allrs2342002
SNP Nexus

SNPshotrs2342002
SNPdbers2342002
MSV3drs2342002
GWAS Ctlgrs2342002
Max Magnitude
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 T
P-val 7E-6
Odds Ratio 1.15 [1.08-1.23]