{{Rsnum
|rsid=17321050
|Gene=TBL1X
|Chromosome=X
|position=9645059
|Orientation=plus
|GMAF=0.214
|Gene_s=TBL1X
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 24.8 | 23.0 | 52.2
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.0 | 100.0
| YRI | 10.9 | 16.3 | 72.8
| ASW | 12.3 | 21.1 | 66.7
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 16.8 | 13.9 | 69.3
| LWK | 13.6 | 14.5 | 71.8
| MEX | 12.1 | 17.2 | 70.7
| MKK | 10.9 | 16.7 | 72.4
| TSI | 25.7 | 15.8 | 58.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=22050706
|Title=An X-chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}