{{Rsnum
|rsid=1322784
|Gene=DISC1
|Chromosome=1
|position=231793189
|Orientation=minus
|GMAF=0.3039
|Gene_s=DISC1,MAP1LC3C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 4.8 | 33.3 | 61.9
| HCB | 13.3 | 55.6 | 31.1
| JPT | 13.6 | 50.0 | 36.4
| YRI | 11.3 | 46.8 | 41.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 13.3 | 55.6 | 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
}}[[rs1322784]], an intragenic SNP associated with the 'disrupted in schizophrenia' DISC1 gene, was reported to be associated with [[asperger's syndrome]] {{PMID|17579608}}

This same study also implicated the "HEP3 haplotype" in [[asperger's syndrome]]. The HEP3 haplotype contains two SNPs in the [[DISC1]] gene, [[rs751229]] and [[rs3738401]], and was first reported as a haplotype under-represented in individuals with affective disorders. [PMID 14532331, PMID 15386212]

{{PMID Auto
|PMID=19414483
|Title=The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}