{{Rsnum
|rsid=2612101
|Gene=ENOSF1
|Chromosome=18
|position=676473
|Orientation=plus
|GMAF=0.197
|Gene_s=ENOSF1
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 57.1 | 33.9 | 8.9
| HCB | 98.5 | 1.5 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 43.2 | 41.8 | 15.1
| ASW | 44.6 | 46.4 | 8.9
| CHB | 98.5 | 1.5 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 89.0 | 11.0 | 0.0
| LWK | 45.5 | 42.7 | 11.8
| MEX | 63.8 | 31.0 | 5.2
| MKK | 51.6 | 41.8 | 6.5
| TSI | 71.3 | 27.7 | 1.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24535845
|Title=Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}