{{Rsnum
|rsid=9392653
|Chromosome=6
|position=5071258
|Orientation=plus
|GMAF=0.2406
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LYRM4
|Gene_s=LYRM4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 54.0 | 38.1 | 8.0
| HCB | 77.4 | 20.4 | 2.2
| JPT | 82.3 | 16.8 | 0.9
| YRI | 37.4 | 51.0 | 11.6
| ASW | 45.6 | 49.1 | 5.3
| CHB | 77.4 | 20.4 | 2.2
| CHD | 89.0 | 11.0 | 0.0
| GIH | 48.5 | 46.5 | 5.0
| LWK | 51.4 | 44.0 | 4.6
| MEX | 50.0 | 39.7 | 10.3
| MKK | 53.2 | 37.2 | 9.6
| TSI | 50.0 | 42.2 | 7.8
| 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=C
  |Pval=2E-9
  |OR=1.74
  |ORtxt=[NR]
  |OA=1
}}

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