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rs6971499

From SNPedia

Orientationplus
Stabilizedplus
Make rs6971499(C;C)
Make rs6971499(C;T)
Make rs6971499(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position130995762
GeneLINC-PINT
is asnp
is mentioned by
dbSNPrs6971499
ebirs6971499
HLIrs6971499
Exacrs6971499
Varsomers6971499
Maprs6971499
PheGenIrs6971499
hapmaprs6971499
1000 genomesrs6971499
hgdprs6971499
ensemblrs6971499
gopubmedrs6971499
geneviewrs6971499
scholarrs6971499
googlers6971499
pharmgkbrs6971499
gwascentralrs6971499
openSNPrs6971499
23andMers6971499
23andMe allrs6971499
SNP Nexus

SNPshotrs6971499
SNPdbers6971499
MSV3drs6971499
GWAS Ctlgrs6971499
Max Magnitude
? (C;C) (C;T) (T;T) 28
A 2014 study "Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer" of 7,683 European cases and 14,397 controls found the minor allele rs6971499(C) in LINC-PINT (long intergenic non-protein coding RNA, p53 induced transcript) conferring a protective effect of statistically genome-wide significance (per-allele odds ratio (OR) = 0.79, 95% confidence interval (CI) 0.74-0.84, P = 3.0E-12) against Pancreatic cancer.


[PMID 25086665OA-icon.png] Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer