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rs9543325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 2 1.37x Slightly higher pancreatic cancer risk
(C;T) 1.37x increased risk of pancreatic cancer
(T;T) normal risk of pancreatic cancer
ReferenceGRCh38 38.1/141
Chromosome13
Position73342491
is asnp
is mentioned by
dbSNPrs9543325
ebirs9543325
HLIrs9543325
Exacrs9543325
Varsomers9543325
Maprs9543325
PheGenIrs9543325
hapmaprs9543325
1000 genomesrs9543325
hgdprs9543325
ensemblrs9543325
gopubmedrs9543325
geneviewrs9543325
scholarrs9543325
googlers9543325
pharmgkbrs9543325
gwascentralrs9543325
openSNPrs9543325
23andMers9543325
23andMe allrs9543325
SNP Nexus

SNPshotrs9543325
SNPdbers9543325
MSV3drs9543325
GWAS Ctlgrs9543325
GMAF0.4766
Max Magnitude2
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20101243OA-icon.png]
Trait Pancreatic cancer
Title A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33
Risk Allele C
P-val 3E-11
Odds Ratio 1.26 [1.18-1.35]

The C allele of this SNP is ssociated with slightly higher risk of pancreatic cancer. [PMID 20101243OA-icon.png]

OMIM260350
Desc
Variant
Relatedalso
[PMID 22665904OA-icon.png] A Replication Study and Genome-wide Scan of Single Nucleotide Polymorphisms Associated with Pancreatic Cancer Risk and Overall Survival


[PMID 20686608OA-icon.png] Genome-wide association study of pancreatic cancer in Japanese population.