{{Rsnum
|rsid=157935
|Gene=LINC-PINT
|Chromosome=7
|position=130900794
|Orientation=plus
|GMAF=0.3301
|Gene_s=LINC-PINT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 8.1 | 38.7 | 53.2
| HCB | 16.8 | 56.2 | 27.0
| JPT | 17.0 | 48.2 | 34.8
| YRI | 3.4 | 35.9 | 60.7
| ASW | 5.3 | 43.9 | 50.9
| CHB | 16.8 | 56.2 | 27.0
| CHD | 19.3 | 51.4 | 29.4
| GIH | 18.8 | 51.5 | 29.7
| LWK | 2.8 | 32.7 | 64.5
| MEX | 10.7 | 33.9 | 55.4
| MKK | 5.8 | 52.6 | 41.7
| TSI | 7.8 | 41.2 | 51.0
| HapMapRevision=28
}}[http://blog.23andme.com/2009/07/06/snpwatch-genetic-variants-near-tumor-suppressor-genes-may-increase-risk-for-brain-and-skin-cancer/ 23andMe blog] [[rs157935]]	T	1.23	[[Basal Cell Carcinoma]] parental imprinting effect
{{PMID Auto
|PMID=19578363
|Title=New common variants affecting susceptibility to basal cell carcinoma
|OA=1
}}

{{omim
|id=613063
|rsnum=157935
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}