{{Rsnum
|rsid=664910
|Gene=MGLL
|Chromosome=3
|position=127755187
|Orientation=plus
|GMAF=0.4417
|Gene_s=MGLL
|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 | 51.3 | 42.5 | 6.2
| HCB | 5.1 | 38.7 | 56.2
| JPT | 7.1 | 37.2 | 55.8
| YRI | 23.8 | 45.6 | 30.6
| ASW | 24.6 | 52.6 | 22.8
| CHB | 5.1 | 38.7 | 56.2
| CHD | 5.5 | 42.2 | 52.3
| GIH | 37.6 | 52.5 | 9.9
| LWK | 17.3 | 47.3 | 35.5
| MEX | 68.4 | 29.8 | 1.8
| MKK | 32.1 | 48.7 | 19.2
| TSI | 50.0 | 39.2 | 10.8
| 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=A
  |Pval=7E-9
  |OR=1.50
  |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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}