{{Rsnum
|rsid=1692120
|Chromosome=11
|position=61650000
|Orientation=plus
|GMAF=0.3136
|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 | 22.1 | 44.2 | 33.6
| HCB | 0.0 | 9.5 | 90.5
| JPT | 0.0 | 7.1 | 92.9
| YRI | 15.6 | 51.0 | 33.3
| ASW | 10.5 | 52.6 | 36.8
| CHB | 0.0 | 9.5 | 90.5
| CHD | 0.0 | 5.5 | 94.5
| GIH | 6.9 | 39.6 | 53.5
| LWK | 23.6 | 47.3 | 29.1
| MEX | 5.2 | 37.9 | 56.9
| MKK | 30.8 | 50.6 | 18.6
| TSI | 27.5 | 42.2 | 30.4
| 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=1E-8
|OR=0.0100
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}