{{Rsnum
|rsid=7179456
|Gene=SLTM
|Chromosome=15
|position=58882340
|Orientation=plus
|GMAF=0.4247
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=SLTM
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 11.5 | 48.7 | 39.8
| HCB | 53.3 | 38.7 | 8.0
| JPT | 62.8 | 32.7 | 4.4
| YRI | 74.8 | 23.8 | 1.4
| ASW | 59.6 | 38.6 | 1.8
| CHB | 53.3 | 38.7 | 8.0
| CHD | 39.4 | 49.5 | 11.0
| GIH | 26.7 | 48.5 | 24.8
| LWK | 80.0 | 19.1 | 0.9
| MEX | 15.5 | 44.8 | 39.7
| MKK | 51.3 | 40.4 | 8.3
| TSI | 5.9 | 49.0 | 45.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21182207
|Trait=None
|Title=Variants in several genomic regions associated with Asperger disorder
|RiskAllele=
|Pval=0.000007
|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}}