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rs11771429

From SNPedia

Orientationplus
Stabilizedplus
Make rs11771429(C;C)
Make rs11771429(C;T)
Make rs11771429(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position153574792
is asnp
is mentioned by
dbSNPrs11771429
ebirs11771429
HLIrs11771429
Exacrs11771429
Varsomers11771429
Maprs11771429
PheGenIrs11771429
hapmaprs11771429
1000 genomesrs11771429
hgdprs11771429
ensemblrs11771429
gopubmedrs11771429
geneviewrs11771429
scholarrs11771429
googlers11771429
pharmgkbrs11771429
gwascentralrs11771429
openSNPrs11771429
23andMers11771429
23andMe allrs11771429
SNP Nexus

SNPshotrs11771429
SNPdbers11771429
MSV3drs11771429
GWAS Ctlgrs11771429
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24121790OA-icon.png]
Trait Barrett's esophagus
Title A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
Risk Allele G
P-val 7E-6
Odds Ratio 1.22 [1.12-1.33]