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rs7904985

From SNPedia

Orientationplus
Stabilizedplus
Make rs7904985(A;A)
Make rs7904985(A;G)
Make rs7904985(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position86356722
GeneGRID1
is asnp
is mentioned by
dbSNPrs7904985
ebirs7904985
HLIrs7904985
Exacrs7904985
Varsomers7904985
Maprs7904985
PheGenIrs7904985
hapmaprs7904985
1000 genomesrs7904985
hgdprs7904985
ensemblrs7904985
gopubmedrs7904985
geneviewrs7904985
scholarrs7904985
googlers7904985
pharmgkbrs7904985
gwascentralrs7904985
openSNPrs7904985
23andMers7904985
23andMe allrs7904985
SNP Nexus

SNPshotrs7904985
SNPdbers7904985
MSV3drs7904985
GWAS Ctlgrs7904985
Max Magnitude
? (A;A) (A;G) (G;G) 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 T
P-val 6E-6
Odds Ratio 1.17 [1.10-1.26]