{{Rsnum
|rsid=2896019
|Gene=PNPLA3
|Chromosome=22
|position=43937814
|Orientation=plus
|GMAF=0.2755
|Gene_s=PNPLA3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 4.4 | 29.2 | 66.4
| HCB | 15.3 | 46.7 | 38.0
| JPT | 23.0 | 43.4 | 33.6
| YRI | 3.4 | 33.3 | 63.3
| ASW | 3.5 | 21.1 | 75.4
| CHB | 15.3 | 46.7 | 38.0
| CHD | 15.6 | 48.6 | 35.8
| GIH | 7.9 | 42.6 | 49.5
| LWK | 1.8 | 18.2 | 80.0
| MEX | 29.3 | 41.4 | 29.3
| MKK | 2.6 | 29.5 | 67.9
| TSI | 2.9 | 29.4 | 67.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23535911
  |Trait=Non-alcoholic fatty liver disease
  |Title=Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.
  |RiskAllele=G
  |Pval=2E-20
  |OR=2.02
  |ORtxt=[1.60-2.56]
  }}

{{PMID Auto
|PMID=22543885
|Title=The association of genetic variants with hepatic steatosis in patients with genotype 1 chronic hepatitis C infection.
|OA=1
}}

{{PMID Auto
|PMID=24831885
|Title=Genetic Variants in the PNPLA3 Gene Are Associated with Nonalcoholic Steatohepatitis
}}

{{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}}