{{Rsnum
|rsid=9821630
|Gene=PLCL2
|Chromosome=3
|position=16929446
|Orientation=plus
|GMAF=0.2998
|Gene_s=PLCL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 53.1 | 38.9 | 8.0
| HCB | 24.1 | 46.0 | 29.9
| JPT | 18.6 | 49.6 | 31.9
| YRI | 95.2 | 4.8 | 0.0
| ASW | 84.2 | 15.8 | 0.0
| CHB | 24.1 | 46.0 | 29.9
| CHD | 16.5 | 47.7 | 35.8
| GIH | 61.4 | 35.6 | 3.0
| LWK | 90.9 | 8.2 | 0.9
| MEX | 43.1 | 48.3 | 8.6
| MKK | 83.3 | 15.4 | 1.3
| TSI | 49.0 | 41.2 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=G
  |Pval=4E-6
  |OR=1.08
  |ORtxt=[1.07-1.1]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}