{{Rsnum
|rsid=2275565
|Gene=MTR
|Chromosome=1
|position=236885376
|Orientation=minus
|GMAF=0.264
|Gene_s=MTR
|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 | 1.8 | 31.0 | 67.3
| HCB | 3.6 | 16.8 | 79.6
| JPT | 7.1 | 31.0 | 61.9
| YRI | 33.3 | 43.5 | 23.1
| ASW | 22.8 | 42.1 | 35.1
| CHB | 3.6 | 16.8 | 79.6
| CHD | 3.7 | 25.9 | 70.4
| GIH | 16.8 | 47.5 | 35.6
| LWK | 28.2 | 45.5 | 26.4
| MEX | 1.7 | 34.5 | 63.8
| MKK | 31.8 | 44.2 | 24.0
| TSI | 3.9 | 31.4 | 64.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23824729
  |Trait=Homocysteine levels
  |Title=Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
  |RiskAllele=T
  |Pval=2E-10
  |OR=.05
  |ORtxt=[0.037-0.072] unit decrease
  }}

{{PMID Auto
|PMID=17903301
|Title=Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.
|OA=1
}}

{{PMID Auto
|PMID=19493349
|Title=118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}