{{Rsnum
|rsid=3830031
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Status = Merged
|Merged = 1263791
|Chromosome=14
|Orientation=plus
|Gene=METTL3
|position=21501530
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=METTL3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 28.6 | 44.6 | 26.8
| HCB | 22.5 | 62.5 | 15.0
| JPT | 23.7 | 60.5 | 15.8
| YRI | 15.3 | 40.7 | 44.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 22.5 | 62.5 | 15.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20523082
|Title=Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population
}}