{{Rsnum
|rsid=7646
|Gene=MTHFD1L
|Chromosome=6
|position=151101614
|Orientation=minus
|GMAF=0.2057
|Gene_s=MTHFD1L
|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 | 12.4 | 38.1 | 49.6
| HCB | 2.9 | 10.3 | 86.8
| JPT | 1.8 | 15.0 | 83.2
| YRI | 1.4 | 25.9 | 72.8
| ASW | 0.0 | 24.6 | 75.4
| CHB | 2.9 | 10.3 | 86.8
| CHD | 0.0 | 8.3 | 91.7
| GIH | 5.0 | 38.6 | 56.4
| LWK | 3.6 | 29.1 | 67.3
| MEX | 5.2 | 44.8 | 50.0
| MKK | 3.2 | 36.5 | 60.3
| TSI | 5.0 | 41.0 | 54.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24123340
|Title=An NTD-Associated Polymorphism in the 3' UTR of MTHFD1L can Affect Disease Risk by Altering miRNA Binding
}}

{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}