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rs1000589

From SNPedia

Orientationplus
Stabilizedplus
Make rs1000589(G;G)
Make rs1000589(G;T)
Make rs1000589(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position63567780
is asnp
is mentioned by
dbSNPrs1000589
ebirs1000589
HLIrs1000589
Exacrs1000589
Varsomers1000589
Maprs1000589
PheGenIrs1000589
hapmaprs1000589
1000 genomesrs1000589
hgdprs1000589
ensemblrs1000589
gopubmedrs1000589
geneviewrs1000589
scholarrs1000589
googlers1000589
pharmgkbrs1000589
gwascentralrs1000589
openSNPrs1000589
23andMers1000589
23andMe allrs1000589
SNP Nexus

SNPshotrs1000589
SNPdbers1000589
MSV3drs1000589
GWAS Ctlgrs1000589
GMAF0.4729
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23180869OA-icon.png]
Trait Pancreatic cancer
Title Genome-wide association study of survival in patients with pancreatic adenocarcinoma.
Risk Allele T
P-val 3E-6
Odds Ratio 1.27 [1.15-1.39]