{{Rsnum
|rsid=7922612
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PLCE1
|position=95811439
|Gene_s=PLCE1
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 43.8 | 47.3 | 8.9
| HCB | 26.3 | 46.7 | 27.0
| JPT | 22.1 | 46.0 | 31.9
| YRI | 4.1 | 36.1 | 59.9
| ASW | 10.5 | 35.1 | 54.4
| CHB | 26.3 | 46.7 | 27.0
| CHD | 26.6 | 55.0 | 18.3
| GIH | 46.5 | 48.5 | 5.0
| LWK | 4.5 | 33.6 | 61.8
| MEX | 63.8 | 29.3 | 6.9
| MKK | 10.3 | 48.1 | 41.7
| TSI | 49.0 | 42.2 | 8.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=24863943
|Title=A multigenic approach to evaluate genetic variants of PLCE1, LXRs, MMPs, TIMP, and CYP genes in gallbladder cancer predisposition
}}

{{PMID Auto
|PMID=24935391
|Title=Phospholipase C Epsilon 1 (PLCE1 rs2274223A&gt;G, rs3765524C&gt;T and rs7922612C&gt;T) Polymorphisms and Esophageal Cancer Risk in the Kashmir Valley
}}

{{PMID Auto
|PMID=25139097
|Title=Role of novel and GWAS originated PLCE1 genetic variants in susceptibility and prognosis of esophageal cancer patients in northern Indian population
}}
{{on chip | Illumina Human 1M}}