{{Rsnum
|rsid=6971499
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LINC-PINT
|position=130995762
|Gene_s=LINC-PINT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 23.0 | 75.2
| HCB | 0.0 | 8.8 | 91.2
| JPT | 0.0 | 7.1 | 92.9
| YRI | 2.7 | 24.5 | 72.8
| ASW | 3.5 | 36.8 | 59.6
| CHB | 0.0 | 8.8 | 91.2
| CHD | 0.0 | 13.8 | 86.2
| GIH | 4.0 | 41.6 | 54.5
| LWK | 2.7 | 22.7 | 74.5
| MEX | 5.2 | 15.5 | 79.3
| MKK | 1.9 | 23.7 | 74.4
| TSI | 2.0 | 24.5 | 73.5
| HapMapRevision=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]].

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}