{{Rsnum
|rsid=1411771
|Gene=DISC1
|Chromosome=1
|position=232039029
|Orientation=plus
|GMAF=0.3517
|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 | 7.1 | 44.2 | 48.7
| HCB | 10.9 | 48.2 | 40.9
| JPT | 8.8 | 38.9 | 52.2
| YRI | 29.3 | 49.7 | 21.1
| ASW | 19.3 | 57.9 | 22.8
| CHB | 10.9 | 48.2 | 40.9
| CHD | 11.9 | 49.5 | 38.5
| GIH | 9.9 | 32.7 | 57.4
| LWK | 29.4 | 53.2 | 17.4
| MEX | 13.8 | 41.4 | 44.8
| MKK | 48.7 | 39.1 | 12.2
| TSI | 8.8 | 47.1 | 44.1
| HapMapRevision=28
}}{{PMID|17673452}} 13 single-nucleotide polymorphisms (SNPs) in 723 members of 179 Finnish [[Bipolar disorder]]  families.
*[[rs751229]](T) and [[rs3738401]](A) was over-transmitted to males with psychotic disorder. 
*under-transmitted [[rs821616]](T) and [[rs1411771]](T)
*The risk haplotype for psychotic disorder also associated to perseverations (P = 0.035; for [[rs751229]] alone P = 0.0012), and a protective haplotype G-T-G with [[rs1655285]] in addition to auditory attention (P = 0.0059).

{{PMID Auto
|PMID=20084519
|Title=Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}