rs9543325

Orientation

plus

Stabilized

plus

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

Reference

GRCh38 38.1/141

Chromosome

13

Position

73342491

is a	snp
is	mentioned by
dbSNP	rs9543325
dbSNP (classic)	rs9543325
ClinGen	rs9543325
ebi	rs9543325
HLI	rs9543325
Exac	rs9543325
Gnomad	rs9543325
Varsome	rs9543325
LitVar	rs9543325
Map	rs9543325
PheGenI	rs9543325
Biobank	rs9543325
1000 genomes	rs9543325
hgdp	rs9543325
ensembl	rs9543325
geneview	rs9543325
scholar	rs9543325
google	rs9543325
pharmgkb	rs9543325
gwascentral	rs9543325
openSNP	rs9543325
23andMe	rs9543325
SNPshot	rs9543325
SNPdbe	rs9543325
MSV3d	rs9543325
GWAS Ctlg	rs9543325

GMAF

0.4766

Max Magnitude

2

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 20101243]
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 20101243]

OMIM	260350
Desc
Variant
Related	also

[PMID 22665904] A Replication Study and Genome-wide Scan of Single Nucleotide Polymorphisms Associated with Pancreatic Cancer Risk and Overall Survival

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

[PMID 28754795] Impact of Sixteen Established Pancreatic Cancer Susceptibility Loci in American Jews.