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rs4800353

From SNPedia

Orientationplus
Stabilizedplus
Make rs4800353(A;A)
Make rs4800353(A;G)
Make rs4800353(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position22074176
is asnp
is mentioned by
dbSNPrs4800353
ebirs4800353
HLIrs4800353
Exacrs4800353
Varsomers4800353
Maprs4800353
PheGenIrs4800353
hapmaprs4800353
1000 genomesrs4800353
hgdprs4800353
ensemblrs4800353
gopubmedrs4800353
geneviewrs4800353
scholarrs4800353
googlers4800353
pharmgkbrs4800353
gwascentralrs4800353
openSNPrs4800353
23andMers4800353
23andMe allrs4800353
SNP Nexus

SNPshotrs4800353
SNPdbers4800353
MSV3drs4800353
GWAS Ctlgrs4800353
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 T
P-val 3E-7
Odds Ratio 1.22 [1.14-1.32]