{{Rsnum
|rsid=419076
|Gene=MECOM
|Chromosome=3
|position=169383098
|Orientation=plus
|GMAF=0.4164
|Gene_s=MECOM
|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 | 31.7 | 48.3 | 20.0
| HCB | 75.0 | 20.5 | 4.5
| JPT | 73.8 | 26.2 | 0.0
| YRI | 14.8 | 57.4 | 27.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 75.0 | 20.5 | 4.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21909115
|Trait=None
|Title=Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|RiskAllele=T
|Pval=2E-13
|OR=0.4090
|ORtxt=[NR] mmHg increase
|OA=1
}}
{{PMID Auto GWAS
|PMID=21909110
|Trait=None
|Title=Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|RiskAllele=T
|Pval=8E-13
|OR=0.3400
|ORtxt=[0.25-0.43] mmHg increase
|OA=1
}}