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rs7632500

From SNPedia

Orientationplus
Stabilizedplus
Make rs7632500(A;A)
Make rs7632500(A;G)
Make rs7632500(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position168007561
is asnp
is mentioned by
dbSNPrs7632500
ebirs7632500
HLIrs7632500
Exacrs7632500
Varsomers7632500
Maprs7632500
PheGenIrs7632500
hapmaprs7632500
1000 genomesrs7632500
hgdprs7632500
ensemblrs7632500
gopubmedrs7632500
geneviewrs7632500
scholarrs7632500
googlers7632500
pharmgkbrs7632500
gwascentralrs7632500
openSNPrs7632500
23andMers7632500
23andMe allrs7632500
SNP Nexus

SNPshotrs7632500
SNPdbers7632500
MSV3drs7632500
GWAS Ctlgrs7632500
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 1E-6
Odds Ratio 1.37 [1.21-1.55]