{{Rsnum
|rsid=4963452
|Chromosome=11
|position=62048331
|Orientation=plus
|GMAF=0.2479
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 26.5 | 73.5
| HCB | 14.1 | 46.7 | 39.3
| JPT | 9.0 | 50.5 | 40.5
| YRI | 0.7 | 20.4 | 78.9
| ASW | 1.8 | 28.1 | 70.2
| CHB | 14.1 | 46.7 | 39.3
| CHD | 10.2 | 48.1 | 41.7
| GIH | 6.9 | 44.6 | 48.5
| LWK | 4.5 | 23.6 | 71.8
| MEX | 21.1 | 47.4 | 31.6
| MKK | 2.6 | 29.5 | 67.9
| TSI | 2.0 | 19.6 | 78.4
| 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=T
|Pval=6E-7
|OR=0.0200
|ORtxt=[NR] % increase
|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}}