{{Rsnum
|rsid=13412852
|Gene=LPIN1
|Chromosome=2
|position=11774815
|Orientation=plus
|GMAF=0.2461
|Gene_s=LPIN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 33.6 | 54.0 | 12.4
| HCB | 66.4 | 30.7 | 2.9
| JPT | 50.4 | 43.4 | 6.2
| YRI | 87.8 | 11.6 | 0.7
| ASW | 89.5 | 10.5 | 0.0
| CHB | 66.4 | 30.7 | 2.9
| CHD | 63.3 | 33.0 | 3.7
| GIH | 63.4 | 33.7 | 3.0
| LWK | 74.5 | 23.6 | 1.8
| MEX | 50.0 | 43.1 | 6.9
| MKK | 62.2 | 35.3 | 2.6
| TSI | 45.1 | 44.1 | 10.8
| HapMapRevision=28
}}

{{PMID Auto
|PMID=18591397
|Title=Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations.
|OA=1
}}

{{PMID Auto
|PMID=22157924
|Title=LPIN1 rs13412852 polymorphism in pediatric nonalcoholic fatty liver disease.
}}

{{on chip | Affy GenomeWide 6}}