{{Rsnum
|rsid=1109748
|Gene=BEST1
|Chromosome=11
|position=61955173
|Orientation=plus
|GMAF=0.2741
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=BEST1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 10.7 | 89.3
| HCB | 54.7 | 34.3 | 10.9
| JPT | 66.4 | 29.2 | 4.4
| YRI | 2.1 | 19.2 | 78.8
| ASW | 0.0 | 12.3 | 87.7
| CHB | 54.7 | 34.3 | 10.9
| CHD | 46.3 | 43.5 | 10.2
| GIH | 26.7 | 59.4 | 13.9
| LWK | 0.9 | 9.1 | 90.0
| MEX | 12.1 | 43.1 | 44.8
| MKK | 0.0 | 3.9 | 96.1
| TSI | 0.0 | 13.7 | 86.3
| 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=5E-9
|OR=0.0500
|ORtxt=[NR] % decrease
|OA=1
}}

{{ClinVar
|ALT=A
|CAF=0.7259; 0.2741
|CHROM=11
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.61722645C>A
|CLNSIG=1
|COMMON=1
|FwdALT=A
|FwdREF=C
|GENEINFO=BEST1:7439
|GENE_ID=7439
|GENE_NAME=BEST1
|REF=C
|RSPOS=61722645
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;MTP
|VC=SNV
|VP=0x050168000000150517120100
|WGT=0
|dbSNPBuildID=86
|rsid=1109748
|CLNACC=RCV000086102.1
|CLNDBN=not provided
|CLNSRC=Retina International
|CLNSRCID=RISN-VMD2:c.219C>A
|Disease=not provided
}}

{{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}}