{{Rsnum
|rsid=9332
|Gene=MTRR
|Chromosome=5
|position=7900599
|Orientation=minus
|GMAF=0.2231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MTRR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 67.3 | 28.3 | 4.4
| HCB | 69.9 | 28.7 | 1.5
| JPT | 77.7 | 21.4 | 0.9
| YRI | 28.8 | 49.3 | 21.9
| ASW | 43.9 | 47.4 | 8.8
| CHB | 69.9 | 28.7 | 1.5
| CHD | 67.6 | 26.9 | 5.6
| GIH | 72.3 | 24.8 | 3.0
| LWK | 34.9 | 54.1 | 11.0
| MEX | 47.4 | 36.8 | 15.8
| MKK | 58.4 | 35.7 | 5.8
| TSI | 66.7 | 31.4 | 2.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19493349
|Title=118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
|OA=1
}}

{{PMID Auto
|PMID=20445798
|Title=Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.
|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}}