{{Rsnum
|rsid=1336708
|Gene=FGF14
|Chromosome=13
|position=102312653
|Orientation=minus
|GMAF=0.2534
|Gene_s=FGF14,FGF14-IT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 36.3 | 58.4
| HCB | 2.9 | 21.2 | 75.9
| JPT | 0.9 | 23.0 | 76.1
| YRI | 20.4 | 55.8 | 23.8
| ASW | 21.1 | 47.4 | 31.6
| CHB | 2.9 | 21.2 | 75.9
| CHD | 3.7 | 31.2 | 65.1
| GIH | 10.9 | 40.6 | 48.5
| LWK | 16.4 | 52.7 | 30.9
| MEX | 3.4 | 32.8 | 63.8
| MKK | 10.9 | 36.5 | 52.6
| TSI | 10.8 | 35.3 | 53.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=
  |Pval=5E-9
  |OR=1.72
  |ORtxt=[NR]
  |OA=1
}}

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