{{Rsnum
|rsid=301443
|Chromosome=9
|position=4594919
|Orientation=minus
|GMAF=0.3384
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SPATA6L
|Gene_s=SPATA6L
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 60.0 | 29.2 | 10.8
| HCB | 22.2 | 46.7 | 31.1
| JPT | 25.0 | 59.1 | 15.9
| YRI | 76.2 | 23.8 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 22.2 | 46.7 | 31.1
| 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=20410850
|Title=Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample
}}{{PMID Auto
|PMID=19152386
|Title=A family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder in 378 families.
}}{{PMID Auto
|PMID=23564280
|Title=Association between SLC1A1 gene and early-onset OCD in the Han Chinese population: a case-control study.
}}

{{PMID Auto
|PMID=23606572
|Title=Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1.
}}
{{PMID Auto
|PMID=23411042
|Title=Association of the candidate gene SLC1A1 and obsessive-compulsive disorder in Han Chinese population
}}