{{Rsnum
|rsid=1367228
|Gene=EFEMP1
|Chromosome=2
|position=55885305
|Orientation=plus
|GMAF=0.3627
|Gene_s=EFEMP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 19.5 | 52.2 | 28.3
| HCB | 83.9 | 16.1 | 0.0
| JPT | 76.1 | 22.1 | 1.8
| YRI | 59.9 | 38.8 | 1.4
| ASW | 52.6 | 35.1 | 12.3
| CHB | 83.9 | 16.1 | 0.0
| CHD | 75.2 | 23.9 | 0.9
| GIH | 42.6 | 47.5 | 9.9
| LWK | 70.0 | 27.3 | 2.7
| MEX | 22.4 | 36.2 | 41.4
| MKK | 62.2 | 34.0 | 3.8
| TSI | 30.4 | 42.2 | 27.5
| 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=T
  |Pval=2E-9
  |OR=1.49
  |ORtxt=[NR]
  |OA=1
}}

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