{{Rsnum
|rsid=3744061
|Gene=MFSD11
|Chromosome=17
|position=76737321
|Orientation=plus
|GMAF=0.4063
|Gene_s=MFSD11,MIR636,SRSF2
|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 | 33.6 | 51.3 | 15.0
| HCB | 23.0 | 50.4 | 26.7
| JPT | 24.8 | 52.2 | 23.0
| YRI | 0.0 | 1.4 | 98.6
| ASW | 1.8 | 24.6 | 73.7
| CHB | 23.0 | 50.4 | 26.7
| CHD | 19.3 | 60.6 | 20.2
| GIH | 16.8 | 43.6 | 39.6
| LWK | 0.9 | 9.2 | 89.9
| MEX | 14.0 | 63.2 | 22.8
| MKK | 2.6 | 31.4 | 66.0
| TSI | 31.4 | 41.2 | 27.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23776548
  |Trait=Retinal arteriolar caliber
  |Title=Genetic loci for retinal arteriolar microcirculation.
  |RiskAllele=G
  |Pval=2E-10
  |OR=.86
  |ORtxt=[0.61-1.11] unit decrease
  |OA=1
}}

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