{{Rsnum
|rsid=13076312
|Gene=LPP
|Chromosome=3
|position=188371466
|Orientation=plus
|GMAF=0.4945
|Gene_s=LPP
|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 | 27.4 | 51.3 | 21.2
| HCB | 16.1 | 47.4 | 36.5
| JPT | 18.6 | 43.4 | 38.1
| YRI | 38.1 | 49.7 | 12.2
| ASW | 33.3 | 49.1 | 17.5
| CHB | 16.1 | 47.4 | 36.5
| CHD | 8.3 | 43.1 | 48.6
| GIH | 14.9 | 55.4 | 29.7
| LWK | 54.5 | 39.1 | 6.4
| MEX | 17.2 | 46.6 | 36.2
| MKK | 45.5 | 39.7 | 14.7
| TSI | 36.3 | 44.1 | 19.6
| HapMapRevision=28
}}[[Generalized Vitiligo]]

{{PMID Auto
|PMID=18311140
|Title=Newly identified genetic risk variants for celiac disease related to the immune response.
|OA=1
}}

{{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}}