{{Rsnum
|rsid=174535
|Gene=MYRF
|Chromosome=11
|position=61783884
|Orientation=plus
|GMAF=0.3567
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYRF
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 12.5 | 43.8 | 43.8
| HCB | 14.1 | 46.7 | 39.3
| JPT | 10.6 | 41.6 | 47.8
| YRI | 1.4 | 18.4 | 80.3
| ASW | 0.0 | 38.6 | 61.4
| CHB | 14.1 | 46.7 | 39.3
| CHD | 28.4 | 43.1 | 28.4
| GIH | 1.0 | 21.8 | 77.2
| LWK | 0.9 | 20.9 | 78.2
| MEX | 42.9 | 44.6 | 12.5
| MKK | 1.9 | 28.2 | 69.9
| TSI | 9.9 | 32.7 | 57.4
| 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=0
|OR=0.0700
|ORtxt=[NR] % increase
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}