{{Rsnum
|rsid=1550976
|Gene=NTM
|Chromosome=11
|position=131450176
|Orientation=plus
|GMAF=0.1823
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NTM
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 49.6 | 44.2 | 6.2
| HCB | 94.2 | 5.8 | 0.0
| JPT | 96.5 | 3.5 | 0.0
| YRI | 75.5 | 22.4 | 2.0
| ASW | 82.5 | 15.8 | 1.8
| CHB | 94.2 | 5.8 | 0.0
| CHD | 96.3 | 3.7 | 0.0
| GIH | 26.7 | 60.4 | 12.9
| LWK | 72.7 | 23.6 | 3.6
| MEX | 50.0 | 37.9 | 12.1
| MKK | 73.1 | 23.1 | 3.8
| TSI | 52.9 | 38.2 | 8.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21182207
|Trait=None
|Title=Variants in several genomic regions associated with Asperger disorder
|RiskAllele=
|Pval=0.000003
|OR=None
|ORtxt=None
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}