{{Rsnum
|rsid=628117
|Gene=NTNG1
|Chromosome=1
|position=107454484
|Orientation=minus
|GMAF=0.3994
|Gene_s=NTNG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 31.0 | 48.7 | 20.4
| HCB | 46.0 | 43.1 | 10.9
| JPT | 49.6 | 42.5 | 8.0
| YRI | 25.9 | 53.1 | 21.1
| ASW | 49.1 | 40.4 | 10.5
| CHB | 46.0 | 43.1 | 10.9
| CHD | 45.9 | 44.0 | 10.1
| GIH | 52.5 | 38.6 | 8.9
| LWK | 26.4 | 48.2 | 25.5
| MEX | 39.7 | 41.4 | 19.0
| MKK | 42.3 | 42.9 | 14.7
| TSI | 35.3 | 47.1 | 17.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=21641949
|Title=Functional variants of the genes involved in neurodevelopment and susceptibility to schizophrenia in an Armenian population
}}

{{PMID|18384956}} Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}