{{Rsnum
|rsid=12091371
|Gene=FMN2
|Chromosome=1
|position=240441752
|Orientation=plus
|GMAF=0.2268
|Gene_s=FMN2
|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 | 0.0 | 14.2 | 85.8
| HCB | 8.8 | 42.3 | 48.9
| JPT | 6.2 | 39.8 | 54.0
| YRI | 21.1 | 55.8 | 23.1
| ASW | 15.8 | 40.4 | 43.9
| CHB | 8.8 | 42.3 | 48.9
| CHD | 18.3 | 42.2 | 39.4
| GIH | 2.0 | 31.7 | 66.3
| LWK | 21.8 | 51.8 | 26.4
| MEX | 3.4 | 19.0 | 77.6
| MKK | 16.0 | 42.9 | 41.0
| TSI | 2.0 | 17.6 | 80.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23535033
  |Trait=Alzheimer's disease (cognitive decline)
  |Title=Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
  |RiskAllele=
  |Pval=7E-8
  |OR=.17
  |ORtxt=unit decrease
  }}

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