{{Rsnum
|rsid=3734398
|Gene=ELOVL2
|Chromosome=6
|position=10982740
|Orientation=plus
|GMAF=0.455
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ELOVL2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 18.6 | 53.1 | 28.3
| HCB | 80.3 | 19.7 | 0.0
| JPT | 77.9 | 22.1 | 0.0
| YRI | 5.4 | 36.1 | 58.5
| ASW | 14.0 | 28.1 | 57.9
| CHB | 80.3 | 19.7 | 0.0
| CHD | 82.6 | 17.4 | 0.0
| GIH | 46.5 | 41.6 | 11.9
| LWK | 5.5 | 35.5 | 59.1
| MEX | 48.3 | 43.1 | 8.6
| MKK | 8.3 | 51.3 | 40.4
| TSI | 19.6 | 55.9 | 24.5
| 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=1E-43
|OR=0.0400
|ORtxt=[NR] % decrease
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}