{{Rsnum
|rsid=3776455
|Gene=MTRR
|Chromosome=5
|position=7896398
|Orientation=minus
|GMAF=0.4871
|Gene_s=MTRR
|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 | 40.7 | 40.7 | 18.6
| HCB | 10.9 | 43.8 | 45.3
| JPT | 11.5 | 46.0 | 42.5
| YRI | 17.8 | 56.2 | 26.0
| ASW | 29.8 | 50.9 | 19.3
| CHB | 10.9 | 43.8 | 45.3
| CHD | 9.2 | 49.5 | 41.3
| GIH | 37.6 | 46.5 | 15.8
| LWK | 22.0 | 52.3 | 25.7
| MEX | 10.3 | 39.7 | 50.0
| MKK | 40.4 | 48.7 | 10.9
| TSI | 31.4 | 50.0 | 18.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=23940529
|Title=Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by bayesian relevance and effect size analysis
|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 v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}