{{Rsnum
|rsid=4552
|Gene=LRP11
|Chromosome=6
|position=149811183
|Orientation=plus
|GMAF=0.3632
|Gene_s=LRP11,PCMT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 38.5 | 53.8 | 7.7
| HCB | 11.1 | 15.6 | 73.3
| JPT | 8.9 | 40.0 | 51.1
| YRI | 0.0 | 25.4 | 74.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 11.1 | 15.6 | 73.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22647835
|Title=Maternal PCMT1 gene polymorphisms and the risk of neural tube defects in a Chinese population of Lvliang high-risk area
}}{{PMID|19290383|OA=1
}} Posttranslational Protein Modifications in Type 1 Diabetes - Genetic Studies with PCMT1, the Repair Enzyme Protein Isoaspartate Methyltransferase (PIMT) Encoding Gene.