{{Rsnum
|rsid=3103778
|Gene=MFSD2A
|Chromosome=1
|position=39968099
|Orientation=plus
|GMAF=0.4761
|Gene_s=MFSD2A
|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 | 21.2 | 50.4 | 28.3
| HCB | 21.9 | 48.2 | 29.9
| JPT | 23.0 | 49.6 | 27.4
| YRI | 60.5 | 32.0 | 7.5
| ASW | 49.1 | 38.6 | 12.3
| CHB | 21.9 | 48.2 | 29.9
| CHD | 17.4 | 51.4 | 31.2
| GIH | 5.9 | 42.6 | 51.5
| LWK | 39.1 | 47.3 | 13.6
| MEX | 20.7 | 62.1 | 17.2
| MKK | 47.4 | 41.7 | 10.9
| TSI | 17.6 | 58.8 | 23.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23534349
  |Trait=PR interval
  |Title=Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
  |RiskAllele=G
  |Pval=9E-6
  |OR=6.30
  |ORtxt=[NR] ms increase
  }}

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