{{Rsnum
|rsid=9851967
|Gene=LPP
|Chromosome=3
|position=188369840
|Orientation=plus
|GMAF=0.3186
|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 | 25.7 | 56.6 | 17.7
| HCB | 43.0 | 47.4 | 9.6
| JPT | 45.0 | 39.6 | 15.3
| YRI | 91.1 | 8.9 | 0.0
| ASW | 78.9 | 19.3 | 1.8
| CHB | 43.0 | 47.4 | 9.6
| CHD | 59.4 | 34.9 | 5.7
| GIH | 59.4 | 34.7 | 5.9
| LWK | 79.6 | 20.4 | 0.0
| MEX | 46.4 | 44.6 | 8.9
| MKK | 64.5 | 30.3 | 5.2
| TSI | 24.5 | 49.0 | 26.5
| HapMapRevision=28
}}[[Celiac Disease]]

{{PMID Auto GWAS
  |PMID=22951725
  |Trait=Vitiligo
  |Title=Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population.
  |RiskAllele=
  |Pval=9E-8
  |OR=1.14
  |ORtxt=[1.09-1.19]
  }}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}