{{Rsnum
|rsid=1391768
|Gene=NDEL1
|Chromosome=17
|position=8437548
|Orientation=minus
|GMAF=0.4109
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NDEL1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 15.0 | 46.0 | 38.9
| HCB | 21.2 | 54.0 | 24.8
| JPT | 10.6 | 45.1 | 44.2
| YRI | 23.1 | 46.9 | 29.9
| ASW | 17.5 | 49.1 | 33.3
| CHB | 21.2 | 54.0 | 24.8
| CHD | 11.0 | 52.3 | 36.7
| GIH | 25.7 | 54.5 | 19.8
| LWK | 22.7 | 47.3 | 30.0
| MEX | 10.3 | 58.6 | 31.0
| MKK | 26.9 | 49.4 | 23.7
| TSI | 7.8 | 47.1 | 45.1
| HapMapRevision=28
}}

{{PMID|18469341|OA=1
}} 275 Caucasian schizophrenia patients and 200 controls [[rs1391768]] imparting a significant effect but only in the context of a Cys carrying background

{{PMID Auto
|PMID=19251251
|Title=Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.
|OA=1
}}

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