{{Rsnum
|rsid=7435
|Gene=AGPAT3
|Chromosome=21
|position=43984457
|Orientation=plus
|GMAF=0.3466
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=AGPAT3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 50.4 | 38.1 | 11.5
| HCB | 45.6 | 46.3 | 8.1
| JPT | 58.9 | 34.8 | 6.2
| YRI | 28.8 | 55.5 | 15.8
| ASW | 38.6 | 42.1 | 19.3
| CHB | 45.6 | 46.3 | 8.1
| CHD | 57.8 | 35.8 | 6.4
| GIH | 30.3 | 53.5 | 16.2
| LWK | 30.9 | 49.1 | 20.0
| MEX | 36.2 | 46.6 | 17.2
| MKK | 31.6 | 47.7 | 20.6
| TSI | 44.6 | 45.5 | 9.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21829377
|Trait=None
|Title=Genetic Loci Associated with Plasma Phospholipid n-3 Fatty Acids: A Meta-Analysis of Genome-Wide Association Studies from the CHARGE Consortium.
|RiskAllele=A
|Pval=2E-7
|OR=0.0200
|ORtxt=[NR] % decrease
|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}}