{{Rsnum
|rsid=157582
|Gene=TOMM40
|Chromosome=19
|position=44892962
|Orientation=plus
|GMAF=0.2773
|Gene_s=TOMM40
|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 | 6.2 | 35.4 | 58.4
| HCB | 0.7 | 40.1 | 59.1
| JPT | 2.7 | 32.7 | 64.6
| YRI | 21.9 | 54.1 | 24.0
| ASW | 17.5 | 45.6 | 36.8
| CHB | 0.7 | 40.1 | 59.1
| CHD | 4.6 | 22.9 | 72.5
| GIH | 5.9 | 22.8 | 71.3
| LWK | 30.0 | 51.8 | 18.2
| MEX | 3.4 | 36.2 | 60.3
| MKK | 18.6 | 46.8 | 34.6
| TSI | 2.0 | 29.4 | 68.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22399527
|Trait=None
|Title=Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
|RiskAllele=T
|Pval=1E-8
|OR=0.1000
|ORtxt=None
|OA=1
}}

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